SCRUBS Foaming Hand Sanitizer
- Product NDC
- 51239-1929
- 11-digit product format
- 512391929
- Labeler code
- 51239
- Product ID
- 51239-1929_5eb2636c-513f-4fdb-9ea4-8ca7270041a0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hand Sanitizer Foam
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- ITW Dymon
- Application
- part333
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2009-10-01
- Marketing end
- 0000-00-00
- Substance
- BENZETHONIUM CHLORIDE; BENZALKONIUM CHLORIDE
- Active strength
- 0 g/970mL; g/970mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 51239-1929-7 | SCRUBS Foaming Hand SanitizerSCRUBS | 252 mL in 1 BOTTLE, PUMP | SOLUTION | 252 | | 15 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51239-1929 | SCRUBS FOAMING HAND SANITIZER SCRUBS (HAND SANITIZER FOAM) SOLUTION [ITW DYMON] | 15 | Legacy NDC, 1 package rows | 20091021_38021d91-5401-4cae-8a93-6114c52d65e0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 51239-1929-7 | 51239192907 | 252 mL in 1 BOTTLE, PUMP | 252 ml | Historical |