Holly and Blu Hand Sanitizer - Candy Apple
- Product NDC
- 87959-001
- 11-digit product format
- 879590001
- Labeler code
- 87959
- Product ID
- 87959-001_5b4c5225-02d1-9ca8-e063-6394a90a3c78
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl Alcohol Gel
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- 8704147 Canada Inc
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-08-29
- Substance
- ALCOHOL
- Active strength
- 62 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Holly and Blu Hand Sanitizer - Candy Apple
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 62 mL/100mL |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87959-001-01 | 87959000101 | 30 mL in 1 BOTTLE, PLASTIC (87959-001-01) | 30 ml | 2026-08-29 | No | No | Current |
| 87959-001-02 | 87959000102 | 1 BOTTLE, SPRAY in 1 POUCH (87959-001-02) / 30 mL in 1 BOTTLE, SPRAY | | 2026-09-12 | No | No | Current |