Hampton Sun SPF50 Mineral Face Sunscreen
- Product NDC
- 87170-012
- 11-digit product format
- 871700012
- Labeler code
- 87170
- Product ID
- 87170-012_51a5c787-c3be-9138-e063-6294a90a747b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Homosalate 7.5%, Octisalate 5.00%, Avobenzone 3.00%
- Dosage form
- STICK
- Route
- TOPICAL
- Labeler
- S&C Hampton Sun LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-12-01
- Substance
- ZINC OXIDE
- Active strength
- 14.69 g/100g
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Hampton Sun SPF50 Mineral Face Sunscreen
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 14.69 g/100g |
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 |
|---|
| 87170-012-01 | Hampton Sun SPF50 Mineral Face Sunscreen | 13 g in 1 CONTAINER | STICK | 13 | | 2 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87170-012-01 | 87170001201 | 13 g in 1 CONTAINER (87170-012-01) | 13 g | 2025-12-01 | No | No | Current |