DANDRUFF CONDITIONER
- Product NDC
- 37808-417
- 11-digit product format
- 378080417
- Labeler code
- 37808
- Product ID
- 37808-417_3dbd14e2-b54c-4f65-a12e-37ae590470d3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- PYRITHIONE ZINC
- Dosage form
- LOTION/SHAMPOO
- Route
- TOPICAL
- Labeler
- HEB
- Application
- part358
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2009-10-20
- Marketing end
- 0000-00-00
- Substance
- PYRITHIONE ZINC
- Active strength
- 1 mL/100mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 37808-417-14 | DANDRUFF CONDITIONER DRY SCALP RECOVERY | 420 mL in 1 BOTTLE, PLASTIC | LOTION/SHAMPOO | 420 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37808-417 | DANDRUFF CONDITIONER (PYRITHIONE ZINC) LOTION/SHAMPOO [HEB] | 1 | Legacy NDC, 1 package rows | 20100223_7f2b9f76-df01-4de5-91d0-6cb29de8bb4c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 37808-417-14 | 37808041714 | 420 mL in 1 BOTTLE, PLASTIC | 420 ml | Historical |