RENEWAL
- Product NDC
- 11822-6221
- 11-digit product format
- 118226221
- Labeler code
- 11822
- Product ID
- 11822-6221_bc4fe34a-bd5e-4983-a681-a62e68581259
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SELENIUM SULFIDE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- RITE AID CORPORATION
- Application
- part358H
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-03-03
- Marketing end
- 0000-00-00
- Substance
- SELENIUM SULFIDE
- Active strength
- 10 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 11822-6221-1 | RENEWALDANDRUFF MOISTURIZING | 325 mL in 1 BOTTLE, PLASTIC | LIQUID | 325 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-6221 | RENEWAL DANDRUFF MOISTURIZING (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION] | 1 | Legacy NDC, 1 package rows | 20150305_bb2b9ff8-ee1f-4532-8e08-62dc21e9bd2b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 11822-6221-1 | 11822622101 | 325 mL in 1 BOTTLE, PLASTIC | 325 ml | Historical |