Acne Scrub
- Product NDC
- 68062-2257
- 11-digit product format
- 680622257
- Labeler code
- 68062
- Product ID
- 68062-2257_48df0eff-9f06-e2fd-e063-6294a90ad526
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- salicylic acid
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Spa de Soleil
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-11-20
- Substance
- SALICYLIC ACID
- Active strength
- 1.8 mg/180mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Acne Scrub
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SALICYLIC ACID | 1.8 mg/180mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O414PZ4LPZ |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68062-2257-1 | Acne Scrub | 120 mL in 1 BOTTLE | LIQUID | 120 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68062-2257 | ACNE SCRUB (SALICYLIC ACID) LIQUID [SPA DE SOLEIL] | 2 | Current NDC, 1 package rows | 20231121_0a9067f7-2a9d-abae-e063-6394a90a3533.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68062-2257-1 | 68062225701 | 120 mL in 1 BOTTLE (68062-2257-1) | 120 ml | 2023-11-20 | No | No | Current |