Over-the-counter medication · Retinoid (Topical)

adapalene

Also sold as Differin.

Data updated 2026-05-15

178,147
FDA reportsHeavily reported
1
InteractionFew interactions
$2.45
Generic price (NADAC)

What the data shows

adapalene (Differin) is an over-the-counter Retinoid (Topical), more reported than roughly 9 in 10 tracked drugs (178,147 FDA reports), with 1 documented drug interaction.

Reporting volume reflects how widely a drug is used and studied, not how dangerous it is, a FAERS report documents a temporal association, never proof of cause.

Drug Pricing (NADAC)

Generic Price

$2.45/unit

Generic Available

Yes (18 manufacturers)

Pricing data from NADAC (CMS), effective December 18, 2024. Compare all drug costs →

NADAC price trail: ADAPALENE 0.1% CREAM

Same CMS presentation as the headline generic unit price above (2 effective dates). Adjacent % compares consecutive NADAC releases for this description only, not a patient out-of-pocket quote. Latest step: +1.7% vs prior release.

Effective NADAC / unit vs prior NDCs
September 18, 2024 $2.41/GM - 1
December 18, 2024 $2.45/GM +1.7% 2
View Alternatives → Compare with Another Drug → Full Side Effects Report →

What it does

Information not available.

Common side effects

Dry skin, Contact dermatitis (skin rash), Burning feeling on the skin where you put the medicine

Key warnings

No specific warnings noted. Always follow your prescriber's instructions.

Side Effects (from patient reports)

Based on 178,147 FDA adverse event reports.

Most-reported reactions

Adverse reactions in FAERS for adapalene, by number of reports

reports

What this shows Bars show how often each reaction was reported, not how likely it is to happen, a report records a temporal association, never proof that the drug caused it.

Source FDA Adverse Event Reporting System (FAERS) As of 2025

Reports over time

Adverse-event reports filed for adapalene each year to the FDA Adverse Event Reporting System (FAERS).

020,00040,00060,00080,000 20042007201020132016201920222025 1,238

Year-to-year volume tracks usage, prescribing, and scrutiny, not a change in per-patient risk. Source: FDA FAERS.

Where adapalene sits

adapalene has more FDA adverse-event reports than 93% of the drugs FAERS tracks. A high position reflects how widely a drug is used and watched, not how dangerous it is.

fewest reports most reports

Percentile across all drugs PlainMeds tracks by FAERS report volume. The dot is adapalene; the line is the median (50th percentile).

FDA Adverse Event Report Analysis

Detailed analysis of 178,147 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2004–2025.

Total Reports

178,147

Reports Mentioning Death

32

0.0% of reports — not proof of cause

Hospitalization Reports

358

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 122,669 (78%)
Male 34,451 (22%)

Age Distribution

0–17 36,553
18–44 43,798
45–64 5,092
65–74 970
75+ 408

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
2 DRY SKIN 44,990
3 SKIN BURNING SENSATION 41,633
4 ACNE 39,264
5 ERYTHEMA 38,379
6 SKIN IRRITATION 26,225
7 SKIN EXFOLIATION 21,251
8 INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION 16,186
9 RASH 15,520
10 OVERDOSE 13,210
11 PAIN OF SKIN 12,283
12 PRURITUS 11,826
13 HYPERSENSITIVITY 8,305
14 UNDERDOSE 4,949
15 CONDITION AGGRAVATED 4,946
16 RASH PAPULAR 4,147

Reactions in Death Reports

DEATH 12
PAIN 5
DYSPNOEA 4
EMOTIONAL DISTRESS 4
WEIGHT DECREASED 4
ANXIETY 3
ASTHMA 3
BONE DENSITY DECREASED 3
COMPLETED SUICIDE 3
CONSTIPATION 3

Reactions in Hospitalization Reports

DYSPNOEA 41
PAIN 41
ANXIETY 39
HYPERSENSITIVITY 32
PULMONARY EMBOLISM 29
FATIGUE 27
DEPRESSION 26
NAUSEA 24
INJURY 23
DIZZINESS 22

Source: FDA FAERS (Adverse Event Reporting System) Reports are voluntary and do not establish causation

Known Drug Interactions

No formal drug-drug interaction studies were conducted with adapalene and benzoyl peroxide gel 0.1% / 2.5%.

Mechanism: There are no known studies showing that these two skin treatments interfere with each other.

This is a plain-language summary of FDA-label interaction records and does not provide individual medication-combination directions.

Common Questions

What are the common side effects of adapalene?
The registry lists Dry skin, Contact dermatitis (skin rash), Burning feeling on the skin where you put the medicine, Skin irritation among the most-reported FAERS reaction terms for adapalene. The compiled record contains 178,147 FDA adverse-event reports. These counts are not an individual symptom assessment.
Does adapalene interact with other medications?
The registry has 1 documented interaction rows for adapalene. Notable source-record pairings include benzoyl peroxide. These rows are not a complete medication review.
What drug class is adapalene?
adapalene belongs to the Retinoid (Topical) drug class. It is available over the counter (OTC).

Other drugs grouped near adapalene - same-class peers and common alternatives.

Compare adapalene vs apremilast side-by-side →

Compare beyond drug class

Nationwide peers by FAERS volume & death-report share

Two PlainMeds-derived comparison paths for adapalene: nearest FDA FAERS report volume and nearest death-report share among drugs with at least 1,000 logged reports, excluding same-class neighbors listed above. Counts reflect reporting volume, not proven individual harm.

Medication Guides

What the FDA Data Shows for adapalene

The FDA label for adapalene (sold under brand names such as Differin) classifies it as an over-the-counter product in the Retinoid (Topical) class. Regulatory labeling describes its approved uses and the patient populations studied in pre-market trials. Official labeling lists 4 commonly reported side effects, including Dry skin, Contact dermatitis (skin rash), Burning feeling on the skin where you put the medicine.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 178,147 voluntary reports. The database also lists 1 documented drug interaction derived from FDA labeling, with the top-flagged interaction rated minor severity. NADAC pricing from CMS shows a generic unit cost of $2.45.

Report counts do not establish causation, a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history, and patent information are separate source-record fields. This page is a public FDA/CMS registry and does not provide medical, treatment, substitution, or medication-change directions.

Data Sources

Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS). Pricing: CMS National Average Drug Acquisition Cost (NADAC).

FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. This registry does not provide medication decisions.

Last updated: January 8, 2025

PlainMeds is rendered directly from FDA openFDA/FAERS extracts, DailyMed labels, and CMS drug-pricing files, no number is typed in by an editor. FAERS counts, recalls, shortages, and price figures on this page are queried live from those federal extracts. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of 2026-05-15. Primary sources: openFDA / FAERS, DailyMed and CMS Part B ASP.

Data currency: FDA FAERS adverse-event reports through 2025, CMS NADAC acquisition-cost pricing effective December 2024, compiled from the source snapshot dated . See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a data issue.

All federal data sources used on this page