5259 HAND SANITIZER
- Product NDC
- 76138-120
- 11-digit product format
- 761380120
- Labeler code
- 76138
- Product ID
- 76138-120_1cee8d76-1f8e-14b4-e063-6294a90afc0e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ETHYL ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Innovation Specialties
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-04-25
- 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
- 5259 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 |
|---|
| 76138-120-04 | 5259 HAND SANITIZER | 40 mL in 1 BOTTLE | GEL | 40 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76138-120 | 5259 HAND SANITIZER (ETHYL ALCOHOL) GEL [INNOVATION SPECIALTIES] | 3 | Current NDC, Legacy NDC, 1 package rows | 20240712_3923fe13-0e57-406a-afb9-3e9cef263dab.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 |
|---|
| 76138-120-04 | 76138012004 | 40 mL in 1 BOTTLE (76138-120-04) | 40 ml | 2019-04-25 | 0000-00-00 | No | No | Current |