SUNSCREEN SPRAY150mL
- Product NDC
- 84938-014
- 11-digit product format
- 849380014
- Labeler code
- 84938
- Product ID
- 84938-014_4635f90a-bbca-0676-e063-6394a90a9f35
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide 12%, Titanium Dioxide 6%, Homosalate 14%, Octisalate 5%
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Foshan Sugar Max Cosmetics CO.,Ltd
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-12-18
- Substance
- HOMOSALATE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- .14; .05; .06; .12 g/mL; g/mL; g/mL; g/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SUNSCREEN SPRAY150mL
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HOMOSALATE | .14 g/mL |
| OCTISALATE | .05 g/mL |
| TITANIUM DIOXIDE | .06 g/mL |
| ZINC OXIDE | .12 g/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V06SV4M95S, 4X49Y0596W, 15FIX9V2JP, SOI2LOH54Z |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84938-014-01 | SUNSCREEN SPRAY150mL | 150 mL in 1 BOTTLE | LIQUID | 150 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84938-014-01 | 84938001401 | 150 mL in 1 BOTTLE (84938-014-01) | 150 ml | 2025-12-18 | No | No | Current |