Walgreens
- Product NDC
- 0363-0859
- 11-digit product format
- 003630859
- Labeler code
- 0363
- Product ID
- 0363-0859_515202a4-edf7-df2c-e063-6294a90ab99a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl Alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Walgreens
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-02-15
- Substance
- ALCOHOL
- Active strength
- 700 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
- Walgreens
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 700 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 581662 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0363-0859-02 | Walgreens | 59 mL in 1 BOTTLE, PLASTIC | GEL | 59 | | 7 |
| 0363-0859-08 | Walgreens | 236 mL in 1 BOTTLE, PLASTIC | GEL | 236 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0363-0859 | WALGREENS (ETHYL ALCOHOL) GEL [WALGREENS] | 4 | Current NDC, 2 package rows | 20250209_eff97d19-8f15-5ea7-e053-2995a90aeae4.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0363-0859-02 | 00363085902 | 59 mL in 1 BOTTLE, PLASTIC (0363-0859-02) | 59 ml | 2023-02-15 | No | No | Current |
| 0363-0859-08 | 00363085908 | 236 mL in 1 BOTTLE, PLASTIC (0363-0859-08) | 236 ml | 2023-02-15 | No | No | Current |