HAND SANITIZER
- Product NDC
- 72580-306
- Requested package NDC
- 72580-306-12
- 11-digit product format
- 725800306
- Labeler code
- 72580
- Product ID
- 72580-306_ceb7f964-c51c-2d74-e053-2995a90af00f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ETHYL ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Formology Lab Inc.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-06-28
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 70 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|---|---|---|---|---|---|---|---|
| 72580-306-12 | 72580030612 | 100 mL in 1 BOTTLE (72580-306-12) | 100 ml | 2020-06-28 | 0000-00-00 | No | No | Current |