Anti-Bacterial Hand Gel
- Product NDC
- 69358-0001
- 11-digit product format
- 693580001
- Labeler code
- 69358
- Product ID
- 69358-0001_4c50d980-5301-4830-814e-311f69550dd6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ETHYL ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- UniGroup Wholesale Inc.
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2014-11-12
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 62 mL/100mL
- 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 |
|---|
| 69358-0001-1 | Anti-Bacterial Hand Gel | 29 mL in 1 BOTTLE, SPRAY | GEL | 29 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69358-0001 | ANTI-BACTERIAL HAND GEL (ETHYL ALCOHOL) GEL [UNIGROUP WHOLESALE INC.] | 1 | Legacy NDC, 1 package rows | 20141112_622cc3f6-81b8-4bae-89bf-cc414a1090c4.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 69358-0001-1 | 69358000101 | 29 mL in 1 BOTTLE, SPRAY | 29 ml | Historical |