Salicylic Acid 6% Gel
- Product NDC
- 59088-216
- 11-digit product format
- 590880216
- Labeler code
- 59088
- Product ID
- 59088-216_52e7c069-a93c-3527-e063-6294a90a984d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SALICYLIC ACID
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- PureTek Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2026-09-10
- Substance
- SALICYLIC ACID
- Active strength
- 6 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Salicylic Acid 6% Gel
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SALICYLIC ACID | 6 g/100g |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 59088-216-03 | 59088021603 | 28.35 g in 1 TUBE (59088-216-03) | 28.35 g | 2026-09-10 | No | No | Current |