foam weightless sunscreen non-tinted drytouch nt

Generic: titanium dioxide, zinc oxide

Labeler: cutis wellness dermatology and dermatopathology pllc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name foam weightless sunscreen non-tinted drytouch nt
Generic Name titanium dioxide, zinc oxide
Labeler cutis wellness dermatology and dermatopathology pllc
Dosage Form AEROSOL, FOAM
Routes
TOPICAL
Active Ingredients

titanium dioxide 30 mg/g, zinc oxide 100 mg/g

Manufacturer
Cutis Wellness Dermatology And Dermatopathology PLLC

Identifiers & Regulatory

Product NDC 85431-211
Product ID 85431-211_45870c56-4bcf-5c3b-e063-6394a90a085c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2023-03-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 85431211
Hyphenated Format 85431-211

Supplemental Identifiers

UNII
15FIX9V2JP SOI2LOH54Z

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name foam weightless sunscreen non-tinted drytouch nt (source: ndc)
Generic Name titanium dioxide, zinc oxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/g
  • 100 mg/g
source: ndc
Packaging
  • 113 g in 1 BOTTLE, PUMP (85431-211-04)
source: ndc

Packages (1)

85431-211-04 113 g in 1 BOTTLE, PUMP (85431-211-04)

Ingredients (2)

titanium dioxide (30 mg/g) zinc oxide (100 mg/g)

Linked Drug Pages (1)

Foam Weightless Sunscreen Non-Tinted Drytouch NT ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "45870c56-4bcf-5c3b-e063-6394a90a085c", "openfda": {"unii": ["15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["335ec22c-6a9a-c4d1-e063-6394a90ac0b0"], "manufacturer_name": ["Cutis Wellness Dermatology And Dermatopathology PLLC"]}, "finished": true, "packaging": [{"sample": false, "description": "113 g in 1 BOTTLE, PUMP (85431-211-04)", "package_ndc": "85431-211-04", "marketing_start_date": "20230315"}], "brand_name": "Foam Weightless Sunscreen Non-Tinted Drytouch NT", "product_id": "85431-211_45870c56-4bcf-5c3b-e063-6394a90a085c", "dosage_form": "AEROSOL, FOAM", "product_ndc": "85431-211", "generic_name": "Titanium Dioxide, Zinc Oxide", "labeler_name": "Cutis Wellness Dermatology And Dermatopathology PLLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Foam Weightless Sunscreen Non-Tinted Drytouch NT", "active_ingredients": [{"name": "TITANIUM DIOXIDE", "strength": "30 mg/g"}, {"name": "ZINC OXIDE", "strength": "100 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230315", "listing_expiration_date": "20261231"}