Scar Gel
- Product NDC
- 54108-8111
- 11-digit product format
- 541088111
- Labeler code
- 54108
- Product ID
- 54108-8111_04ff8c03-d928-4bfd-88d5-3bf14b9da3c9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- derma e
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-07-15
- Substance
- ZINC OXIDE
- Active strength
- 117 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
- Scar Gel
- Brand name suffix
- SPF 35
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 117 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | SOI2LOH54Z |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 54108-8111-1 | Scar GelSPF 35 | 1 in 1 BOX | CREAM | 1 | | 1 |
| 54108-8111-1 | Scar GelSPF 35 | 43 g in 1 TUBE | CREAM | 43 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 54108-8111 | SCAR GEL SPF 35 (ZINC OXIDE) CREAM [DERMA E] | 1 | Current NDC, 2 package rows | 20240816_8cd263aa-a54b-4c55-b3e2-6f6763987d4a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 54108-8111-1 | 54108811101 | 1 TUBE in 1 BOX (54108-8111-1) / 43 g in 1 TUBE | 1 tube | 2020-07-15 | No | No | Historical |