Foaming Alcohol Hand Sanitizer
- Product NDC
- 78641-688
- Requested package NDC
- 78641-688-78
- 11-digit product format
- 786410688
- Labeler code
- 78641
- Product ID
- 78641-688_d6e3fa45-f21e-f2dd-e053-2a95a90a1ccb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl Alcohol
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Global Equipment Company
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-16
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 62 mL/100mL
- 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.
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 78641-688-78 | 78641068878 | 950 mL in 1 BOTTLE (78641-688-78) | 950 ml | 2020-03-16 | 0000-00-00 | No | No | Current |