Acne Treatment
- Product NDC
- 76162-229
- 11-digit product format
- 761620229
- Labeler code
- 76162
- Product ID
- 76162-229_4ab82269-281c-d203-e063-6394a90ae996
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzoyl peroxide
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Topco Associates LLC
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-08-23
- Substance
- BENZOYL PEROXIDE
- Active strength
- 100 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
- Acne Treatment
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOYL PEROXIDE | 100 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W9WZN9A0GM |
| Rxcui | 486131 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76162-229-10 | Acne Treatment | 28 g in 1 TUBE | GEL | 28 | | 6 |
| 76162-229-10 | Acne Treatment | 1 in 1 PACKAGE | GEL | 1 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76162-229 | ACNE TREATMENT (BENZOYL PEROXIDE) GEL [TOPCO ASSOCIATES LLC] | 4 | Current NDC, Legacy NDC, 2 package rows | 20240919_8d5e7e40-5e61-470a-b8ff-0b2dca3cabb0.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 |
|---|
| 76162-229-10 | 76162022910 | 1 TUBE in 1 PACKAGE (76162-229-10) / 28 g in 1 TUBE | 1 tube | 2022-08-23 | 0000-00-00 | No | No | Current |