Hand Sanitizer
- Product NDC
- 76138-114
- 11-digit product format
- 761380114
- Labeler code
- 76138
- Product ID
- 76138-114_1cee8656-3017-15b2-e063-6394a90a1e1d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Innovation Specialties Inc
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2016-01-02
- Substance
- ALCOHOL
- Active strength
- 62 mL/100mL
- 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 | 62 mL/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 581660 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76138-114-13 | Hand Sanitizer | 30 mL in 1 BOTTLE | GEL | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76138-114 | HAND SANITIZER (ETHYL ALCOHOL) GEL [INNOVATION SPECIALTIES INC] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240712_b2eee632-5a1d-4df5-99c8-8ceb3d644c94.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 |
|---|
| 76138-114-13 | 76138011413 | 30 mL in 1 BOTTLE (76138-114-13) | 30 ml | 2016-01-02 | 0000-00-00 | No | No | Current |