Salicylic Acid
- Product NDC
- 69256-036
- 11-digit product format
- 692560036
- Labeler code
- 69256
- Product ID
- 69256-036_40abb868-3ae2-6d34-e063-6294a90a8afe
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Liquid Corn and Callus Remover
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Harris Teeter, LLC
- Application
- M030
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2017-12-21
- Substance
- SALICYLIC ACID
- Active strength
- .17 mg/9.8mL
- 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 mg/9.8mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O414PZ4LPZ |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69256-036-09 | Salicylic Acid | 9.8 mL in 1 PACKAGE | LIQUID | 9.8 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69256-036 | SALICYLIC ACID (LIQUID CORN AND CALLUS REMOVER) LIQUID [HARRIS TEETER, LLC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241212_27a1c74d-f983-4e18-9854-7a83c3365c85.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69256-036-09 | 69256003609 | 9.8 mL in 1 PACKAGE (69256-036-09) | 9.8 ml | 2017-12-21 | 0000-00-00 | No | No | Current |