Wart Remover Gel
- Product NDC
- 56104-237
- 11-digit product format
- 561040237
- Labeler code
- 56104
- Product ID
- 56104-237_32d28d8e-c7ac-2e09-e063-6294a90aee0a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Wart Remover Gel
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Premier Brands of America Inc.
- Application
- M028
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2013-01-01
- Substance
- SALICYLIC ACID
- Active strength
- .17 g/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Wart Remover Gel
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SALICYLIC ACID | .17 g/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O414PZ4LPZ |
| Rxcui | 312880 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 56104-237-07 | Wart Remover Gel | 7 g in 1 TUBE | GEL | 7 | | 11 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 56104-237 | WART REMOVER GEL GEL [PREMIER BRANDS OF AMERICA INC.] | 11 | Current NDC, Legacy NDC, 1 package rows | 20250417_db4ba7ac-a58b-42d5-9181-da70309f1791.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 56104-237-07 | 56104023707 | 7 g in 1 TUBE (56104-237-07) | 7 g | 2013-01-01 | 0000-00-00 | No | No | Current |