Medicated Apricot Scrub
- Product NDC
- 41163-041
- 11-digit product format
- 411630041
- Labeler code
- 41163
- Product ID
- 41163-041_4af6bd00-f6d4-b7ee-e063-6394a90a591e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Salicylic acid
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- United Natural Foods, Inc. dba UNFI
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2015-07-06
- Substance
- SALICYLIC ACID
- Active strength
- 20 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Medicated Apricot Scrub
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SALICYLIC ACID | 20 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O414PZ4LPZ |
| Rxcui | 562600 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 41163-041-30 | Medicated Apricot Scrub | 170 g in 1 TUBE | GEL | 170 | | 17 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41163-041 | MEDICATED APRICOT SCRUB (SALICYLIC ACID) GEL [UNITED NATURAL FOODS, INC. DBA UNFI] | 15 | Current NDC, Legacy NDC, 1 package rows | 20240310_677c19eb-780b-479b-ab1d-df249e0af6ea.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 |
|---|
| 41163-041-30 | 41163004130 | 170 g in 1 TUBE (41163-041-30) | 170 g | 2015-07-06 | 0000-00-00 | No | No | Current |