Walgreens Acne Control Gel
- Product NDC
- 0363-0269
- 11-digit product format
- 003630269
- Labeler code
- 0363
- Product ID
- 0363-0269_24729761-e0eb-0a70-e063-6394a90affcf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SALICYLIC ACID
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- WALGREEN COMPANY
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-05-02
- Substance
- SALICYLIC ACID
- Active strength
- 20 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
- Walgreens Acne Control Gel
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SALICYLIC ACID | 20 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O414PZ4LPZ |
| Rxcui | 346298 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0363-0269-83 | Walgreens Acne Control Gel | 40 mL in 1 TUBE | GEL | 40 | | 2 |
| 0363-0269-83 | Walgreens Acne Control Gel | 1 in 1 CARTON | GEL | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0363-0269 | WALGREENS ACNE CONTROL GEL (SALICYLIC ACID) GEL [WALGREEN COMPANY] | 2 | Current NDC, 2 package rows | 20241016_ffc4c35b-1390-951b-e053-6294a90a1b11.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 |
|---|
| 0363-0269-83 | 00363026983 | 1 TUBE in 1 CARTON (0363-0269-83) / 40 mL in 1 TUBE | 1 tube | 2023-05-02 | No | No | Current |