FORGESKIN
- Product NDC
- 87604-001
- 11-digit product format
- 876040001
- Labeler code
- 87604
- Product ID
- 87604-001_4fa7e67d-cfc6-9f73-e063-6394a90ada50
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MINERAL TALLOW SUNSCREEN
- Dosage form
- CREAM
- Route
- CUTANEOUS
- Labeler
- GUANGZHOU KANGLIXIN BIOTECHNOLOGY CO.,LTD
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-04-17
- Substance
- ZINC OXIDE
- Active strength
- 250 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- FORGESKIN
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 250 mg/mL |
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 |
|---|
| 87604-001-01 | FORGESKIN | 80 mL in 1 BOTTLE | CREAM | 80 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87604-001-01 | 87604000101 | 80 mL in 1 BOTTLE (87604-001-01) | 80 ml | 2026-04-17 | No | No | Current |