Miracle Brands Hand Sanitizer
- Product NDC
- 79779-001
- 11-digit product format
- 797790001
- Labeler code
- 79779
- Product ID
- 79779-001_d58e8113-87b6-6b76-e053-2a95a90a2a46
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol Free Hand Sanitizer
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Kelly Products, Inc.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-08-19
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 79779-001-01 | 79779000101 | 3785 g in 1 BOTTLE, SPRAY (79779-001-01) | 3785 g | 2020-08-19 | 0000-00-00 | No | No | Current |
| 79779-001-04 | 79779000104 | 118 g in 1 BOTTLE, SPRAY (79779-001-04) | 118 g | 2020-08-19 | 0000-00-00 | No | No | Current |
| 79779-001-08 | 79779000108 | 236 g in 1 BOTTLE, SPRAY (79779-001-08) | 236 g | 2020-08-19 | 0000-00-00 | No | No | Current |