Salicylic Acid
- Product NDC
- 36800-043
- 11-digit product format
- 368000043
- Labeler code
- 36800
- Product ID
- 36800-043_42f4c6e4-ceb8-dd92-e063-6294a90ac1c5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Wart Remover Gel
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Topco Associates LLC
- Application
- M028
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2014-10-07
- Substance
- SALICYLIC ACID
- Active strength
- .17 g/7g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Salicylic Acid
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SALICYLIC ACID | .17 g/7g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O414PZ4LPZ |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 36800-043-25 | Salicylic Acid | 7 g in 1 TUBE | GEL | 7 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 36800-043 | SALICYLIC ACID (WART REMOVER GEL) GEL [TOPCO ASSOCIATES LLC] | 7 | Current NDC, Legacy NDC, 1 package rows | 20241215_a03fca7c-eeb3-40f9-93bc-1aeb6e06a3cc.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 36800-043-25 | 36800004325 | 7 g in 1 TUBE (36800-043-25) | 7 g | 2014-10-07 | 0000-00-00 | No | No | Current |