HAND SANITIZER
- Product NDC
- 77239-101
- Requested package NDC
- 77239-101-11
- 11-digit product format
- 772390101
- Labeler code
- 77239
- Product ID
- 77239-101_d772cf43-d253-7043-e053-2a95a90a9eb3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ETHYL ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Maapilim Usa, Inc.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-05-04
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 70 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 |
|---|
| 77239-101-11 | 77239010111 | 100 mL in 1 TUBE (77239-101-11) | 100 ml | 2020-05-04 | 0000-00-00 | No | No | Current |