Salicylic Acid
- Product NDC
- 49035-018
- 11-digit product format
- 490350018
- Labeler code
- 49035
- Product ID
- 49035-018_38419bec-6b0e-994e-e063-6394a90adcc4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Liquid Corn and Callus Remover
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Wal-Mart Stores, Inc.
- Application
- M030
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2014-03-04
- Marketing end
- 2026-06-30
- Substance
- SALICYLIC ACID
- Active strength
- .17 g/g
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Salicylic Acid
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SALICYLIC ACID | .17 g/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O414PZ4LPZ |
| Rxcui | 312881 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 49035-018-09 | Salicylic Acid | 9 g in 1 BOTTLE, WITH APPLICATOR | LIQUID | 9 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49035-018 | SALICYLIC ACID (LIQUID CORN AND CALLUS REMOVER) LIQUID [WAL-MART STORES, INC.] | 9 | Current NDC, Legacy NDC, 1 package rows | 20241219_b68e81a3-51c8-4dcb-9cb7-8d8d22983b81.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 |
|---|
| 49035-018-09 | 49035001809 | 9 g in 1 BOTTLE, WITH APPLICATOR (49035-018-09) | 9 g | 2014-03-04 | 2026-06-30 | No | No | Current |