Smarties Hand Sanitizer
- Product NDC
- 72308-023
- 11-digit product format
- 723080023
- Labeler code
- 72308
- Product ID
- 72308-023_ac0da716-f23a-62f5-e053-2a95a90a4bf4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl Alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Flex Beauty Labs
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-08-03
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 1 mL/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 72308-023-39 | Smarties Hand Sanitizer | 39 mL in 1 BOTTLE | GEL | 39 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72308-023 | SMARTIES HAND SANITIZER (ETHYL ALCOHOL) GEL [FLEX BEAUTY LABS] | 2 | Legacy NDC, 1 package rows | 20200805_455c93a0-6de1-4636-8cbe-b50d8b1ee524.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 |
|---|
| 72308-023-39 | 72308002339 | 39 mL in 1 BOTTLE (72308-023-39) | 39 ml | 2020-08-03 | 0000-00-00 | No | No | Current |