Salicylic Acid
- Product NDC
- 0363-0219
- 11-digit product format
- 003630219
- Labeler code
- 0363
- Product ID
- 0363-0219_42f4cafa-14cf-06b2-e063-6394a90aa119
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Wart Remover Gel
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Walgreen Company
- Application
- M028
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2012-08-24
- 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 |
|---|
| 0363-0219-25 | 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 |
|---|
| 0363-0219 | SALICYLIC ACID (WART REMOVER GEL) GEL [WALGREEN COMPANY] | 7 | Current NDC, Legacy NDC, 1 package rows | 20241207_9d73b428-b6a0-4b11-88b7-36c012d24e62.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0363-0219-25 | 00363021925 | 7 g in 1 TUBE (0363-0219-25) | 7 g | 2012-08-24 | 0000-00-00 | No | No | Current |