Salicylic acid
- Product NDC
- 41163-135
- 11-digit product format
- 411630135
- Labeler code
- 41163
- Product ID
- 41163-135_47423642-9b4e-0e15-e063-6294a90a5edc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Medicated Callus Removers Extra Thick
- Dosage form
- PATCH
- Route
- TOPICAL
- Labeler
- United Natural Foods, Inc. dba UNFI
- Application
- M030
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2017-12-27
- Substance
- SALICYLIC ACID
- Active strength
- 40 mg/41
- 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 | 40 mg/41 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O414PZ4LPZ |
| Rxcui | 240559 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 41163-135-04 | Salicylic acid | 4 in 1 PACKAGE | PATCH | 4 | | 10 |
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 |
|---|
| 41163-135-04 | 41163013504 | 4 PATCH in 1 PACKAGE (41163-135-04) | 4 patch | 2017-12-27 | 0000-00-00 | No | No | Current |