Walgreens Acne Foaming Wash
- Product NDC
- 0363-1522
- 11-digit product format
- 003631522
- Labeler code
- 0363
- Product ID
- 0363-1522_d786a02f-5c87-452e-8145-08b90a2f5e9c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzoyl Peroxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Walgreen Company
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-03-15
- Substance
- BENZOYL PEROXIDE
- Active strength
- 100 mg/g
- 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 Foaming Wash
- Brand name suffix
- Acne Medication
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOYL PEROXIDE | 100 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W9WZN9A0GM |
| Rxcui | 142034 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0363-1522-01 | Walgreens Acne Foaming WashAcne Medication | 156 g in 1 TUBE | LOTION | 156 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0363-1522 | WALGREENS ACNE FOAMING WASH ACNE MEDICATION (BENZOYL PEROXIDE) LOTION [WALGREEN COMPANY] | 2 | Current NDC, Legacy NDC, 1 package rows | 20241102_f34affe9-d470-48a5-b0d1-d62b9c44b3f2.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 |
|---|
| 0363-1522-01 | 00363152201 | 156 g in 1 TUBE (0363-1522-01) | 156 g | 2019-03-15 | 0000-00-00 | No | No | Current |