Salicylic Acid
- Product NDC
- 70000-0332
- 11-digit product format
- 700000332
- Labeler code
- 70000
- Product ID
- 70000-0332_4745ad6c-8db6-18af-e063-6394a90a0814
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Liquid Corn and Callus Remover
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- LEADER/ Cardinal Health 110, Inc.
- Application
- M030
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-02-02
- Substance
- SALICYLIC ACID
- Active strength
- 17 g/100mL
- 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/100mL |
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 |
|---|
| 70000-0332-1 | Salicylic Acid | 9.8 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 9.8 | | 15 |
| 70000-0332-1 | Salicylic Acid | 1 in 1 CARTON | LIQUID | 1 | | 15 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70000-0332 | SALICYLIC ACID (LIQUID CORN AND CALLUS REMOVER) LIQUID [LEADER/ CARDINAL HEALTH 110, INC.] | 12 | Current NDC, Legacy NDC, 2 package rows | 20241103_61edf291-cf65-4b57-b9b0-c6204c446f0b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70000-0332-1 | 70000033201 | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (70000-0332-1) / 9.8 mL in 1 BOTTLE, WITH APPLICATOR | 2018-02-02 | 0000-00-00 | No | No | Current |