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Medical Disclaimer: This information is for educational purposes only and is not a substitute for professional medical advice.
Adapalene And Benzoyl Peroxide Gel, 0.1%/2.5%
Brand Name
Adapalene And Benzoyl Peroxide Gel, 0.1%/2.5%
Generic Name
Adapalene And Benzoyl Peroxide Gel, 0.1%/2.5%
Active Ingredient
AdapaleneCategory
Retinoid [EPC]
Variants
3
Different strengths and dosage forms
| Strength | Form | Route | NDC |
|---|---|---|---|
| 1 mg/g | GEL | TOPICAL | 21922-052 |
| 1 mg/g | GEL | TOPICAL | 72162-2296 |
| 1 mg/g | GEL | TOPICAL | 82429-313 |
This page is for informational purposes only and does not replace medical advice. Before using any prescription or over-the-counter medication for Adapalene And Benzoyl Peroxide Gel, 0.1%/2.5%, you must consult a qualified healthcare professional.
Detailed information about Adapalene And Benzoyl Peroxide Gel, 0.1%/2.5%
Adapalene is a third-generation topical retinoid used primarily for the treatment of acne vulgaris by modulating cellular differentiation and keratinization.
For the treatment of acne vulgaris, the standard adult dosage is a thin film of Adapalene (0.1% or 0.3%) applied once daily to the affected areas. It is typically applied in the evening before bedtime. Clinical efficacy is usually observed after 8 to 12 weeks of consistent use. Using more than the recommended amount will not speed up results and may significantly increase the risk of severe skin irritation.
Because systemic absorption of topical adapalene is negligible, no dosage adjustments are required for patients with kidney disease. However, patients should always inform their doctor of their medical history.
Similarly, due to minimal systemic exposure, no specific dosage adjustments are recommended for patients with liver impairment.
Clinical studies of adapalene did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently than younger subjects. In general, elderly patients may have thinner, more fragile skin, so healthcare providers may recommend less frequent application initially to monitor for irritation.
Adapalene is for external (topical) use only. It should never be taken by mouth or applied to mucous membranes (inside the nose or mouth).
If you miss a dose, apply it as soon as you remember. However, if it is almost time for your next dose, skip the missed dose and resume your regular schedule. Do not 'double up' or apply extra medication to make up for a missed application, as this will likely cause skin peeling and redness.
Acute systemic overdose from topical application is highly unlikely. If the medication is applied excessively, it will result in marked redness, peeling, and discomfort. In the event of accidental oral ingestion, contact a Poison Control Center immediately. While adapalene has low systemic toxicity, ingestion of large amounts could theoretically lead to symptoms similar to Vitamin A toxicity (hypervitaminosis A), such as nausea, headache, and dizziness.
> Important: Follow your healthcare provider's dosing instructions. Do not adjust your dose without medical guidance.
During the first 2 to 4 weeks of treatment, most patients experience what is colloquially known as the 'retinoid purge' or 'acneization.' This is a period where the skin adjusts to the medication. Common symptoms include:
These symptoms usually peak at the two-week mark and gradually subside as the skin develops 'retinization' (tolerance to the retinoid).
Adapalene is a powerful dermatological agent that must be used with caution. The most critical safety point is the protection of the skin barrier. Patients should avoid using 'harsh' skincare products such as abrasive soaps, chemical exfoliants (AHAs, BHAs), or astringents while using adapalene, as these can compound irritation and lead to skin damage.
No FDA black box warnings for Adapalene. It is categorized as a safe topical medication when used as directed on the label or by a physician.
There are no absolute systemic contraindications for topical adapalene, but the following topical combinations should be avoided to prevent severe skin damage:
Adapalene must NEVER be used in the following circumstances:
These conditions require a careful risk-benefit analysis by a healthcare provider:
Adapalene is classified by the FDA as Pregnancy Category C. This means that animal reproduction studies have shown an adverse effect on the fetus when administered orally at high doses, but there are no adequate and well-controlled studies in humans. Because topical absorption is minimal, the risk is likely low. However, because retinoids as a class are potentially teratogenic (causing birth defects), healthcare providers generally advise women to discontinue adapalene as soon as pregnancy is confirmed or when planning to conceive.
It is not known whether topical adapalene is excreted in human milk. Because systemic absorption is so low, it is considered unlikely to pose a significant risk to a nursing infant. However, caution should be exercised. To minimize risk, do not apply adapalene to the chest or nipple area to prevent the infant from coming into direct contact with the medication or ingesting it.
Adapalene is approved for use in children aged 12 years and older. Its use in younger children is generally not recommended because their skin barrier is different, and the safety profile has not been rigorously studied in this age group. In adolescents, it is a first-line treatment for acne, but parents should monitor for proper application and sun protection.
Adapalene is a chemically stable, retinoid-like compound. It acts by binding to specific retinoic acid nuclear receptors (RAR), particularly the beta and gamma subtypes. Unlike tretinoin, it does not bind to the cytosolic retinoic acid-binding proteins (CRABP). By binding to these nuclear receptors, adapalene alters the transcription of genes involved in cell differentiation and inflammation. It normalizes the keratinization process in the sebaceous follicle, preventing the formation of microcomedones and promoting the drainage of existing comedones.
Adapalene's primary effect is comedolytic and anti-inflammatory. It reduces the 'stickiness' of follicular skin cells. The onset of action is slow; while some anti-inflammatory effects may be seen in 1-2 weeks, the full comedolytic effect requires 8 to 12 weeks of continuous therapy. It does not have any direct antibacterial properties and does not affect sebum production levels directly.
| Parameter | Value |
|---|---|
Common questions about Adapalene And Benzoyl Peroxide Gel, 0.1%/2.5%
Adapalene is primarily used for the topical treatment of acne vulgaris in adults and children 12 years of age and older. It works by normalizing the growth and shedding of skin cells within the pores, which prevents the formation of blackheads and whiteheads. Additionally, it has anti-inflammatory properties that help reduce the redness and swelling of pimples. While mainly for acne, some doctors may use it off-label for conditions like keratosis pilaris or fine wrinkles. It is available both over-the-counter and by prescription depending on the strength.
The most common side effects include skin dryness, redness, scaling, and a mild burning or stinging sensation. These symptoms are most frequent during the first two to four weeks of treatment as the skin adjusts to the medication. This period is often called 'purging' because acne may temporarily seem to get worse before it gets better. Most of these side effects are manageable with a gentle moisturizer and typically decrease after a month of use. If irritation becomes severe, you should consult your healthcare provider about reducing the frequency of application.
There is no known direct interaction between topical adapalene and alcohol consumption. Unlike certain oral medications, adapalene is applied to the skin and very little of it enters the bloodstream. However, alcohol can cause systemic dehydration, which may lead to drier skin and make the local irritation from adapalene feel more uncomfortable. It is generally safe to consume alcohol in moderation, but maintaining skin hydration is important. Always follow the specific advice provided by your healthcare professional regarding lifestyle choices during treatment.
Adapalene is generally not recommended for use during pregnancy. While systemic absorption through the skin is very low, retinoids as a class are known to potentially cause birth defects when taken orally. Because there are no definitive studies proving its safety in pregnant women, most doctors advise stopping the medication if you become pregnant or are planning to conceive. It is classified as Pregnancy Category C by the FDA. You should discuss alternative acne treatments that are considered safer during pregnancy with your dermatologist.
Adapalene is not an overnight fix and requires consistent use to see results. Most patients begin to see a noticeable improvement in their skin after 8 to 12 weeks of daily application. During the first few weeks, your acne might actually appear to worsen as the medication clears out deep-seated clogs. It is important not to get discouraged and to continue using the product as directed. If you do not see any improvement after three months, consult your doctor to discuss whether a different treatment or a higher concentration is needed.
Yes, you can stop using adapalene suddenly without experiencing physical withdrawal symptoms. However, because adapalene works by regulating skin cell turnover, stopping it may cause your acne to return over time. Many people use adapalene as a long-term maintenance therapy to keep their skin clear. If you wish to stop, it is often better to gradually reduce the frequency of use rather than quitting all at once. Consult with your healthcare provider to create a long-term plan for maintaining your skin health after your acne has cleared.
If you miss a dose of adapalene, apply it as soon as you remember. If it is already the next day or close to the time of your next scheduled dose, skip the missed dose entirely. Do not apply a double amount of the gel to make up for the missed application. Applying too much adapalene in a short period will not make it work faster and will likely result in significant skin irritation, redness, and peeling. Simply return to your normal once-daily evening routine.
No, topical adapalene does not cause weight gain. Because the medication is applied only to the skin and systemic absorption is negligible, it does not affect your metabolism, hormones, or appetite. Weight changes are not listed as a side effect in any clinical trials for adapalene. If you are experiencing unexplained weight gain while using this medication, it is likely due to other factors or medications. You should discuss any concerns about weight changes with your primary care physician.
Adapalene can be used alongside many other medications, but you must be careful with other topical skin products. Using it with other irritating agents like salicylic acid, sulfur, or high concentrations of benzoyl peroxide can lead to severe skin peeling. It is generally safe to use with oral antibiotics or oral contraceptives often prescribed for acne. Always provide your doctor with a full list of your current medications, including over-the-counter supplements. They can help you coordinate a skincare routine that minimizes the risk of adverse interactions.
Yes, adapalene is widely available as a generic medication. The 0.1% gel was the first to become available as a generic and is also available over-the-counter under various brand names and store labels. The 0.3% gel and certain cream formulations may still require a prescription but are also available in generic forms. Generic adapalene contains the same active ingredient and meets the same FDA standards for efficacy and safety as the brand-name versions like Differin. Choosing the generic version is often a more cost-effective way to treat acne.
Other drugs with the same active ingredient (Adapalene)
> Warning: Stop taking Adapalene and call your doctor immediately if you experience any of these.
Adapalene is generally considered safe for long-term use. There is no evidence that long-term use 'thins' the skin in a harmful way; in fact, retinoids are known to support collagen production in the deeper dermis. However, chronic irritation can lead to a compromised skin barrier, making the skin more reactive to other skincare products or environmental factors. Regular use of sunscreen is mandatory during long-term therapy to prevent cumulative UV damage to the sensitized skin.
No FDA black box warnings currently exist for Adapalene. Unlike oral isotretinoin (Accutane), topical adapalene does not carry a black box warning for birth defects or psychiatric issues, due to its minimal systemic absorption. However, it should still be used with caution and under professional supervision.
Report any unusual symptoms to your healthcare provider. If skin irritation becomes severe or interferes with daily life, your doctor may recommend reducing application to every other night or switching to a lower concentration.
Unlike oral acne medications, topical adapalene does not require routine blood tests (such as liver enzymes or lipid panels). Monitoring is primarily clinical:
Adapalene has no known effect on the ability to drive or operate machinery. It does not cause drowsiness or impair cognitive function.
There are no direct drug-alcohol interactions with topical adapalene. However, excessive alcohol consumption can dehydrate the skin, potentially making the irritation from adapalene feel more pronounced.
Adapalene does not cause physical dependence or withdrawal. However, stopping the medication abruptly may lead to a recurrence of acne lesions. Many dermatologists recommend a 'tapering' approach for maintenance—reducing application from every night to 2-3 times a week once the skin is clear.
> Important: Discuss all your medical conditions with your healthcare provider before starting Adapalene.
There are no known food interactions with topical adapalene. Unlike oral Vitamin A supplements, dietary intake of fats or specific fruits does not affect the absorption or efficacy of the topical gel.
Adapalene is not known to interfere with standard blood or urine laboratory tests. Its presence in the blood is too low to affect biochemical assays.
Mechanism of Interaction: Most interactions with adapalene are 'pharmacodynamic' and localized to the skin. They involve additive irritation rather than changes in liver metabolism. The management strategy usually involves staggering the application of different products or reducing the frequency of use.
> Important: Tell your doctor about ALL medications, supplements, and herbal products you are taking.
Patients who have had severe reactions to other retinoids (like tretinoin or tazarotene) are more likely to experience sensitivity with adapalene, though many find adapalene more tolerable. There is no known cross-reactivity with non-retinoid medications.
> Important: Your healthcare provider will evaluate your complete medical history before prescribing Adapalene.
Acne is less common in the elderly, but adapalene may be used for other conditions. Older patients often have thinner skin (atrophy) and decreased sebum production, which can make them more susceptible to the irritating effects of retinoids. A 'low and slow' approach (starting with 0.1% cream every third night) is often recommended.
No dose adjustment is needed for patients with renal impairment. The drug does not accumulate in the system even with impaired kidney function due to the negligible amounts that reach the bloodstream.
No dose adjustment is needed for patients with hepatic impairment. While the liver is responsible for processing absorbed retinoids, the topical dose of adapalene is insufficient to cause concern in patients with liver disease.
> Important: Special populations require individualized medical assessment.
| Protein Binding | >99% (primarily to albumin) |
| Half-life | Not established (minimal systemic levels) |
| Tmax | 8 to 15 hours (if detectable) |
| Metabolism | Primarily O-demethylation and hydroxylation (Liver) |
| Excretion | Biliary (Fecal) >95% |
Adapalene is a third-generation topical retinoid. It is more photostable and lipophilic than first-generation retinoids (like tretinoin) and second-generation retinoids (like etretinate). It is often grouped with tazarotene and trifarotene as modern, receptor-selective retinoids.