DOP Ethyl Alcohol 70%
- Product NDC
- 51048-048
- 11-digit product format
- 510480048
- Labeler code
- 51048
- Product ID
- 51048-048_28caf8eb-1b93-4d28-b12d-22c5eda9bf8a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl Alcohol
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Omega & Delta Co., Inc.
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-01-01
- Substance
- ALCOHOL
- Active strength
- 70 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
- DOP Ethyl Alcohol 70%
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 70 mL/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 582753 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51048-048-16 | DOP Ethyl Alcohol 70% | 473 mL in 1 BOTTLE, PLASTIC | LIQUID | 473 | | 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 |
|---|
| 51048-048-16 | 51048004816 | 473 mL in 1 BOTTLE, PLASTIC (51048-048-16) | 473 ml | 2023-01-01 | No | No | Historical |