Alcohol
- Product NDC
- 73884-001
- 11-digit product format
- 738840001
- Labeler code
- 73884
- Product ID
- 73884-001_a1629152-276f-8040-e053-2a95a90a25da
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Pop Fizz Designs
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-09-20
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 62 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 73884-001-11 | 73884000111 | 10 BOTTLE in 1 BOX (73884-001-11) > 29 mL in 1 BOTTLE (73884-001-01) | 10 bottle | 2022-09-20 | 0000-00-00 | No | No | Current |