Hand Sanitizer
- Product NDC
- 76544-710
- 11-digit product format
- 765440710
- Labeler code
- 76544
- Product ID
- 76544-710_a3e68fd1-57da-6781-e053-2a95a90af6e1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Great White Bottling Inc
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-30
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 80 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76544-710-12 | Hand Sanitizer | 355 mL in 1 BOTTLE | GEL | 355 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76544-710 | HAND SANITIZER (ALCOHOL) GEL [GREAT WHITE BOTTLING INC] | 1 | Legacy NDC, 1 package rows | 20200428_a3e78f97-82ad-7cdf-e053-2a95a90a91a4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76544-710-12 | 76544071012 | 355 mL in 1 BOTTLE (76544-710-12) | 355 ml | 2020-03-30 | 0000-00-00 | No | No | Current |