ETHYL ALCOHOL
- Product NDC
- 83986-973
- 11-digit product format
- 839860973
- Labeler code
- 83986
- Product ID
- 83986-973_4cc5cc94-9acd-fb3f-e063-6394a90a8d3b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ethyl alcohol
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- UpLift Brands, LLC
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-11-03
- Substance
- ALCOHOL
- Active strength
- 62 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ETHYL ALCOHOL
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 62 mL/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 247835 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 83986-973-16 | ETHYL ALCOHOL | 59 mL in 1 BOTTLE, PLASTIC | LIQUID | 59 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 83986-973-16 | 83986097316 | 59 mL in 1 BOTTLE, PLASTIC (83986-973-16) | 59 ml | 2025-11-03 | No | No | Historical |