Foam Weightless Sunscreen Non-Tinted Drytouch NT
- Product NDC
- 85431-211
- 11-digit product format
- 854310211
- Labeler code
- 85431
- Product ID
- 85431-211_45870c56-4bcf-5c3b-e063-6394a90a085c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Titanium Dioxide, Zinc Oxide
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- Cutis Wellness Dermatology And Dermatopathology PLLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-03-15
- Substance
- TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 30; 100 mg/g; 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
- Foam Weightless Sunscreen Non-Tinted Drytouch NT
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TITANIUM DIOXIDE | 30 mg/g |
| ZINC OXIDE | 100 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 15FIX9V2JP, SOI2LOH54Z |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85431-211-04 | Foam Weightless Sunscreen Non-Tinted Drytouch NT | 113 g in 1 BOTTLE, PUMP | AEROSOL, FOAM | 113 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 85431-211 | FOAM WEIGHTLESS SUNSCREEN NON-TINTED DRYTOUCH NT (TITANIUM DIOXIDE, ZINC OXIDE) AEROSOL, FOAM [CUTIS WELLNESS DERMATOLOGY AND DERMATOPATHOLOGY PLLC] | 1 | Current NDC, 1 package rows | 20250424_335ec22c-6a9a-c4d1-e063-6394a90ac0b0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85431-211-04 | 85431021104 | 113 g in 1 BOTTLE, PUMP (85431-211-04) | 113 g | 2023-03-15 | No | No | Historical |