mineral sunscreen dry touch 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 mineral sunscreen dry touch nt
Generic Name titanium dioxide, zinc oxide
Labeler cutis wellness dermatology and dermatopathology pllc
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

titanium dioxide 80 mg/g, zinc oxide 38 mg/g

Manufacturer
Cutis Wellness Dermatology And Dermatopathology PLLC

Identifiers & Regulatory

Product NDC 85431-202
Product ID 85431-202_458708b4-56b7-8d18-e063-6294a90a8c47
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2022-10-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 85431202
Hyphenated Format 85431-202

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 mineral sunscreen dry touch nt (source: ndc)
Generic Name titanium dioxide, zinc oxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 80 mg/g
  • 38 mg/g
source: ndc
Packaging
  • 53 g in 1 BOTTLE, PUMP (85431-202-50)
source: ndc

Packages (1)

85431-202-50 53 g in 1 BOTTLE, PUMP (85431-202-50)

Ingredients (2)

titanium dioxide (80 mg/g) zinc oxide (38 mg/g)

Linked Drug Pages (1)

Mineral Sunscreen Dry Touch NT ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "458708b4-56b7-8d18-e063-6294a90a8c47", "openfda": {"unii": ["15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["334ffc49-3196-0995-e063-6394a90ad559"], "manufacturer_name": ["Cutis Wellness Dermatology And Dermatopathology PLLC"]}, "finished": true, "packaging": [{"sample": false, "description": "53 g in 1 BOTTLE, PUMP (85431-202-50)", "package_ndc": "85431-202-50", "marketing_start_date": "20221028"}], "brand_name": "Mineral Sunscreen Dry Touch NT", "product_id": "85431-202_458708b4-56b7-8d18-e063-6294a90a8c47", "dosage_form": "CREAM", "product_ndc": "85431-202", "generic_name": "Titanium Dioxide, Zinc Oxide", "labeler_name": "Cutis Wellness Dermatology And Dermatopathology PLLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mineral Sunscreen Dry Touch NT", "active_ingredients": [{"name": "TITANIUM DIOXIDE", "strength": "80 mg/g"}, {"name": "ZINC OXIDE", "strength": "38 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221028", "listing_expiration_date": "20261231"}