Advanced Hand Sanitizer
- Product NDC
- 72308-001
- 11-digit product format
- 723080001
- Labeler code
- 72308
- Product ID
- 72308-001_6b9e574c-36b7-553a-e053-2991aa0ae65b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- HAND SANITIZER
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Flex Beauty Labs, LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-08-02
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 62 mL/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 72308-001-01 | Advanced Hand Sanitizer | 295 mL in 1 BOTTLE, PLASTIC | LIQUID | 295 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72308-001 | ADVANCED HAND SANITIZER (HAND SANITIZER) LIQUID [FLEX BEAUTY LABS, LLC] | 2 | Legacy NDC, 1 package rows | 20180507_5a5562eb-9864-46cf-a35e-d11741166f53.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 72308-001-01 | 72308000101 | 295 mL in 1 BOTTLE, PLASTIC | 295 ml | Historical |