B-Pure Hand Sanitizer Vanilla Honey Scented
- Product NDC
- 80684-205
- 11-digit product format
- 806840205
- Labeler code
- 80684
- Product ID
- 80684-205_4e090205-c774-1666-e063-6394a90a8287
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Fourstar Group USA, Inc.
- Application
- 505(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-03-12
- Substance
- ALCOHOL
- Active strength
- 70 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
- B-Pure Hand Sanitizer Vanilla Honey Scented
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 70 mL/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 1041849 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 80684-205-01 | B-Pure Hand Sanitizer Vanilla Honey Scented | 10 mL in 1 BOTTLE | LIQUID | 10 | | 1 |
| 80684-205-02 | B-Pure Hand Sanitizer Vanilla Honey Scented | 59 mL in 1 BOTTLE | LIQUID | 59 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 80684-205-01 | 80684020501 | 10 mL in 1 BOTTLE (80684-205-01) | 10 ml | 2026-03-12 | No | No | Current |
| 80684-205-02 | 80684020502 | 59 mL in 1 BOTTLE (80684-205-02) | 59 ml | 2026-03-12 | No | No | Current |