3-pack Dark Hand Sanitizer
- Product NDC
- 85782-030
- 11-digit product format
- 857820030
- Labeler code
- 85782
- Product ID
- 85782-030_5d55c878-a04a-ddf5-e063-6294a90a13f0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Isopropyl Alcohol
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- handetizer, LLC
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-10-08
- Substance
- ISOPROPYL ALCOHOL
- Active strength
- 72 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
- 3-pack Dark Hand Sanitizer
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ISOPROPYL ALCOHOL | 72 mL/100mL |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 85782-030-01 | 85782003001 | 3 BOTTLE, SPRAY in 1 BOX (85782-030-01) / 20 mL in 1 BOTTLE, SPRAY | 2026-10-08 | No | No | Current |