Anti Bacterial Hand Gel
- Product NDC
- 62670-6701
- 11-digit product format
- 626706701
- Labeler code
- 62670
- Product ID
- 62670-6701_4c9bf5b8-83b9-f9f6-e063-6294a90a8559
- 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
- 2024-05-31
- 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
- Sea and Sandstone
- 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 |
|---|
| 62670-6701-0 | Anti Bacterial Hand GelSea and Sandstone | 29 mL in 1 BOTTLE | GEL | 29 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62670-6701 | ANTI BACTERIAL HAND GEL SEA AND SANDSTONE (ALCOHOL) GEL [BATH & BODY WORKS, INC.] | 1 | Current NDC, 1 package rows | 20240627_1bbaa2b3-9322-9aab-e063-6394a90a14c9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 62670-6701-0 | 62670670100 | 29 mL in 1 BOTTLE (62670-6701-0) | 29 ml | 2024-05-31 | No | No | Historical |