HAND SANITIZER
- Product NDC
- 72580-309
- 11-digit product format
- 725800309
- Labeler code
- 72580
- Product ID
- 72580-309_ceb86245-edfb-1596-e053-2a95a90ac640
- 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
- 2020-08-25
- 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
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 |
|---|
| 72580-309-01 | 72580030901 | 1.5 mL in 1 POUCH (72580-309-01) | 1.5 ml | 2020-08-25 | 0000-00-00 | No | No | Current |
| 72580-309-03 | 72580030903 | 3 mL in 1 POUCH (72580-309-03) | 3 ml | 2020-08-25 | 0000-00-00 | No | No | Current |