Dermatouch Acnecare Facial Scrub
- Product NDC
- 68062-2255
- 11-digit product format
- 680622255
- Labeler code
- 68062
- Product ID
- 68062-2255_48dfccec-6fcf-1369-e063-6394a90a3e0f
- 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
- 2023-08-07
- 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
- Dermatouch Acnecare Facial 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 |
|---|
| 68062-2255-1 | Dermatouch Acnecare Facial Scrub | 180 mL in 1 BOTTLE | LIQUID | 180 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68062-2255 | DERMATOUCH ACNECARE FACIAL SCRUB (SALICYLIC ACID) LIQUID [SPA DE SOLEIL] | 1 | Current NDC, 1 package rows | 20230808_025d4242-9e7d-9ba1-e063-6294a90af752.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68062-2255-1 | 68062225501 | 180 mL in 1 BOTTLE (68062-2255-1) | 180 ml | 2023-08-07 | No | No | Current |