SAFEWAY
- Product NDC
- 21130-620
- 11-digit product format
- 211300620
- Labeler code
- 21130
- Product ID
- 21130-620_a4a72e34-da4e-4ac9-9a86-20fc3092b183
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SELENIUM SULFIDE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- SAFEWAY INC.
- Application
- part358H
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2013-06-20
- 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 |
|---|
| 21130-620-11 | SAFEWAY | 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 |
|---|
| 21130-620 | SAFEWAY (SELENIUM SULFIDE) LIQUID [SAFEWAY INC.] | 1 | Legacy NDC, 1 package rows | 20130624_fb9d7e17-b289-4ad6-a4ba-64a4a1397663.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 21130-620-11 | 21130062011 | 325 mL in 1 BOTTLE, PLASTIC | 325 ml | Historical |