Anti Bacterial Hand Gel
- Product NDC
- 62670-6937
- 11-digit product format
- 626706937
- Labeler code
- 62670
- Product ID
- 62670-6937_4cac74b6-e579-ea96-e063-6394a90a54ef
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Bath & Body Works, Inc.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-10-20
- Substance
- ALCOHOL
- Active strength
- 71 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Anti Bacterial Hand Gel
- Brand name suffix
- Pure Wonder
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 71 mL/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 2282911 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62670-6937-0 | Anti Bacterial Hand GelPure Wonder | 29 mL in 1 BOTTLE | GEL | 29 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 62670-6937-0 | 62670693700 | 29 mL in 1 BOTTLE (62670-6937-0) | 29 ml | 2025-10-20 | No | No | Historical |