Ethyl Alcohol
- Product NDC
- 83986-471
- 11-digit product format
- 839860471
- Labeler code
- 83986
- Product ID
- 83986-471_5035ec52-2d66-cbbf-e063-6294a90a4a5c
- 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
- 2026-04-24
- 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 |
|---|
| 83986-471-16 | Ethyl Alcohol | 59 mL in 1 BOTTLE, PLASTIC | LIQUID | 59 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 83986-471-16 | 83986047116 | 59 mL in 1 BOTTLE, PLASTIC (83986-471-16) | 59 ml | 2026-04-24 | No | No | Historical |