HAND SANITIZER
- Product NDC
- 79631-000
- 11-digit product format
- 796310000
- Labeler code
- 79631
- Product ID
- 79631-000_0899cafe-9050-8a8e-e063-6394a90a1f0e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Andaz Group LLC
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-07-18
- Substance
- ALCOHOL
- Active strength
- .75 mL/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- HAND SANITIZER
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | .75 mL/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 1305100 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 79631-000-00 | HAND SANITIZER | 35 mL in 1 BOTTLE | GEL | 35 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 79631-000 | HAND SANITIZER (ALCOHOL) GEL [ANDAZ GROUP LLC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231026_5033fcad-fb65-45b8-a4ec-c7b2c9d11793.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 79631-000-00 | 79631000000 | 35 mL in 1 BOTTLE (79631-000-00) | 35 ml | 2020-07-18 | 0000-00-00 | No | No | Current |