Benzoyl Peroxide 5% Gel
- Product NDC
- 68723-305
- 11-digit product format
- 687230305
- Labeler code
- 68723
- Product ID
- 68723-305_e5a2beb3-04a4-47e4-87a2-e66f6ee04407
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzoyl Peroxide
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Axia Medical Solutions, LLC
- Application
- part333D
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-07-18
- Marketing end
- 0000-00-00
- Substance
- BENZOYL PEROXIDE
- Active strength
- 50 mg/1000mg
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68723-305-02 | Benzoyl Peroxide 5% Gel | 57 mg in 1 BOTTLE, PLASTIC | GEL | 57 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68723-305 | BENZOYL PEROXIDE 5% GEL (BENZOYL PEROXIDE) GEL [AXIA MEDICAL SOLUTIONS, LLC] | 4 | Legacy NDC, 1 package rows | 20210713_a0e4581a-ea6b-4c82-998f-4ea4103c857b.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 |
|---|
| 68723-305-02 | 68723030502 | 57 mg in 1 BOTTLE, PLASTIC (68723-305-02) | 57 mg | 2017-07-18 | 0000-00-00 | No | No | Current |