Liquid Callus Remover
- Product NDC
- 56104-501
- 11-digit product format
- 561040501
- Labeler code
- 56104
- Product ID
- 56104-501_40aba81a-36f9-82cc-e063-6394a90a3b06
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Salicylic Acid
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Premier Brands of America Inc.
- Application
- M030
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-09-11
- Substance
- SALICYLIC ACID
- Active strength
- 170 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Liquid Callus Remover
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SALICYLIC ACID | 170 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O414PZ4LPZ |
| Rxcui | 312881 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 56104-501-00 | Liquid Callus Remover | 1 in 1 CARTON | LIQUID | 1 | | 4 |
| 56104-501-00 | Liquid Callus Remover | 9.8 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 9.8 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 56104-501 | LIQUID CALLUS REMOVER (SALICYLIC ACID) LIQUID [PREMIER BRANDS OF AMERICA INC.] | 3 | Current NDC, 2 package rows | 20241016_051c7917-76ea-c7f8-e063-6394a90a9e36.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 56104-501-00 | 56104050100 | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (56104-501-00) / 9.8 mL in 1 BOTTLE, WITH APPLICATOR | 2023-09-11 | No | No | Historical |