Dandruff
- Product NDC
- 76162-353
- 11-digit product format
- 761620353
- Labeler code
- 76162
- Product ID
- 76162-353_4ab83628-a6a6-c90d-e063-6394a90a1f28
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pyrithione zinc
- Dosage form
- SHAMPOO
- Route
- TOPICAL
- Labeler
- Topco Associates LLC
- Application
- M032
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-10-25
- Substance
- PYRITHIONE ZINC
- Active strength
- 10 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dandruff
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PYRITHIONE ZINC | 10 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | R953O2RHZ5 |
| Rxcui | 209884 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76162-353-32 | Dandruff | 370 mL in 1 BOTTLE, PLASTIC | SHAMPOO | 370 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76162-353 | DANDRUFF (PYRITHIONE ZINC) SHAMPOO [TOPCO ASSOCIATES LLC] | 2 | Current NDC, 1 package rows | 20241027_a0f2c58b-bb17-42a3-bd90-be771f60ef20.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 76162-353-32 | 76162035332 | 370 mL in 1 BOTTLE, PLASTIC (76162-353-32) | 370 ml | 2024-10-25 | No | No | Historical |