Choice
- Product NDC
- 58575-183
- 11-digit product format
- 585750183
- Labeler code
- 58575
- Product ID
- 58575-183_11db4e3e-c442-4134-b4d3-23aa6ebc081e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl Alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Inopak. Ltd
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-01-02
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 70 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 58575-183-01 | 58575018301 | 800 mL in 1 POUCH (58575-183-01) | 800 ml | 2020-01-02 | 0000-00-00 | No | No | Current |
| 58575-183-02 | 58575018302 | 9600 mL in 1 CASE (58575-183-02) | 9600 ml | 2020-01-02 | 0000-00-00 | No | No | Current |