Acne Control Face Wash
- Product NDC
- 54111-185
- 11-digit product format
- 541110185
- Labeler code
- 54111
- Product ID
- 54111-185_12333d48-9807-48dc-bdd9-a7b19b77374a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SALICYLIC ACID
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Bentley Laboratories, LLC
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-12-01
- Substance
- SALICYLIC ACID
- Active strength
- 2 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Acne Control Face Wash
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SALICYLIC ACID | 2 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O414PZ4LPZ |
| Rxcui | 562600 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 54111-185-01 | Acne Control Face Wash | 180 mL in 1 BOTTLE | GEL | 180 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 54111-185 | ACNE CONTROL FACE WASH (SALICYLIC ACID) GEL [BENTLEY LABORATORIES, LLC] | 1 | Current NDC, 1 package rows | 20241202_068c5fef-cdc5-49f4-9372-9cfdd07508b8.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 |
|---|
| 54111-185-01 | 54111018501 | 180 mL in 1 BOTTLE (54111-185-01) | 180 ml | 2024-12-01 | No | No | Current |