Ethyl Alcohol
- Product NDC
- 73762-070
- 11-digit product format
- 737620070
- Labeler code
- 73762
- Product ID
- 73762-070_e3b1aef0-4d8b-4b32-84c7-ad022a87c3f7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl Alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- RESQUE1ST LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-23
- 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 |
|---|
| 73762-070-08 | 73762007008 | 236 mL in 1 BOTTLE, PUMP (73762-070-08) | 236 ml | 2020-03-23 | 0000-00-00 | No | No | Current |