Anti-BacterialHandSpray
- Product NDC
- 62670-6791
- 11-digit product format
- 626706791
- Labeler code
- 62670
- Product ID
- 62670-6791_4c1030b5-469a-dd98-e063-6294a90a9d7d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Bath & Body Works, Inc.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-08-26
- Marketing end
- 2028-03-01
- Substance
- ALCOHOL
- Active strength
- 72 mL/100mL
- NDC exclude flag
- No
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 3K9958V90M | ALCOHOL | 64-17-5 | ALCOHOL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 62670-6791-2 | 62670679102 | 29 mL in 1 BOTTLE, SPRAY (62670-6791-2) | 29 ml | 2024-08-26 | 2028-03-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| 1oz ABHS Lavender and Vanilla | Bath & Body Works, Inc. | Tri Tech Laboratories LLC | 2026-03-02 | HUMAN OTC DRUG LABEL | 2 |