Ethyl Rubbing Alcohol
- Product NDC
- 0395-0040
- 11-digit product format
- 003950040
- Labeler code
- 0395
- Product ID
- 0395-0040_0c92880c-76b6-b96f-e063-6394a90a7c31
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Humco Holding Group, Inc.
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1997-01-01
- Substance
- ALCOHOL
- Active strength
- 700 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ethyl Rubbing Alcohol
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 700 mg/mL |
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 |
|---|
| 0395-0040-16 | Ethyl Rubbing Alcohol | 473 mL in 1 BOTTLE, PLASTIC | LIQUID | 473 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0395-0040 | ETHYL RUBBING ALCOHOL (ALCOHOL) LIQUID [HUMCO HOLDING GROUP, INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20231216_829f3e16-7a9b-4da7-87d2-f58254bda721.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0395-0040-16 | 00395004016 | 473 mL in 1 BOTTLE, PLASTIC (0395-0040-16) | 473 ml | 1997-01-01 | 0000-00-00 | No | No | Current |