Alcohol
- Product NDC
- 41190-849
- 11-digit product format
- 411900849
- Labeler code
- 41190
- Product ID
- 41190-849_4aba72f4-4663-6d36-e063-6294a90affe8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Wakefern Food Corp.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-06-21
- Substance
- ALCOHOL
- Active strength
- 62 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Alcohol
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 62 mg/mL |
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 |
|---|
| 41190-849-16 | Alcohol | 59 mL in 1 BOTTLE, PLASTIC | LIQUID | 59 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41190-849 | ALCOHOL LIQUID [WAKEFERN] | 4 | Current NDC, Legacy NDC, 1 package rows | 20250515_c5dd2b25-9003-4c4b-8a86-ecf186695ce3.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 |
|---|
| 41190-849-16 | 41190084916 | 59 mL in 1 BOTTLE, PLASTIC (41190-849-16) | 59 ml | 2022-06-21 | 0000-00-00 | No | No | Current |