SAFEWAY
- Product NDC
- 21130-294
- 11-digit product format
- 211300294
- Labeler code
- 21130
- Product ID
- 21130-294_fbcce930-35ca-4feb-85f5-60986137ccf3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TRICLOSAN
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- SAFEWAY INC.
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2012-01-03
- Marketing end
- 0000-00-00
- Substance
- TRICLOSAN
- Active strength
- 0 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 |
|---|
| 21130-294-64 | SAFEWAY | 1890 mL in 1 BOTTLE, PLASTIC | LIQUID | 1890 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21130-294 | SAFEWAY (TRICLOSAN) LIQUID [SAFEWAY INC.] | 1 | Legacy NDC, 1 package rows | 20120127_969a1508-df2c-4557-8742-61e793374f54.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 21130-294-64 | 21130029464 | 1890 mL in 1 BOTTLE, PLASTIC | 1890 ml | Historical |