Hand Sanitizer
- Product NDC
- 72707-001
- 11-digit product format
- 727070001
- Labeler code
- 72707
- Product ID
- 72707-001_7ba62c4e-b39a-a614-e053-2a91aa0a1d64
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZETHONIUM CHLORIDE
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- DISNEY DESTINATIONS,LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-11-27
- Marketing end
- 0000-00-00
- Substance
- BENZETHONIUM CHLORIDE
- Active strength
- 0 g/100mL
- 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 |
|---|
| 72707-001-01 | Hand Sanitizer | 29 mL in 1 BOTTLE, PLASTIC | GEL | 29 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72707-001 | HAND SANITIZER (BENZETHONIUM CHLORIDE) GEL [DISNEY DESTINATIONS,LLC] | 1 | Legacy NDC, 1 package rows | 20181127_7ba62c4e-b399-a614-e053-2a91aa0a1d64.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 72707-001-01 | 72707000101 | 29 mL in 1 BOTTLE, PLASTIC | 29 ml | Historical |