BENZOYL PEROXIDE 5% / NIACINAMIDE 2% / TRETINOIN 0.025%
- Product NDC
- 72934-1021
- 11-digit product format
- 729341021
- Labeler code
- 72934
- Product ID
- 72934-1021_a73176b0-b460-3810-e053-2995a90a97be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BENZOYL PEROXIDE 5% / NIACINAMIDE 2% / TRETINOIN 0.025%
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Sincerus, Florida, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2019-05-03
- Marketing end
- 0000-00-00
- Substance
- BENZOYL PEROXIDE; NIACINAMIDE; TRETINOIN
- Active strength
- 5 g/100g; g/100g; g/100g
- Pharmacologic classes
- Retinoid [EPC],Retinoids [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 72934-1021-2 | BENZOYL PEROXIDE 5% / NIACINAMIDE 2% / TRETINOIN 0.025% | 30 g in 1 BOTTLE, PUMP | GEL | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72934-1021 | BENZOYL PEROXIDE 5% / NIACINAMIDE 2% / TRETINOIN 0.025% GEL [SINCERUS, FLORIDA, LLC] | 2 | Legacy NDC, 1 package rows | 20200604_87ee6153-34bd-164d-e053-2a95a90a91e1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72934-1021-2 | 72934102102 | 30 g in 1 BOTTLE, PUMP (72934-1021-2) | 30 g | 2019-05-03 | 0000-00-00 | No | No | Current |