Package 85431-211-04

Brand: foam weightless sunscreen non-tinted drytouch nt

Generic: titanium dioxide, zinc oxide
NDC Package

Package Facts

Identity

Package NDC 85431-211-04
Digits Only 8543121104
Product NDC 85431-211
Product ID 85431-211_45870c56-4bcf-5c3b-e063-6394a90a085c
Description

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

Marketing

Marketing Status
Marketed Since 2023-03-15
Brand foam weightless sunscreen non-tinted drytouch nt
Generic titanium dioxide, zinc oxide
Sample Package No

Linked Drug Pages (1)

Foam Weightless Sunscreen Non-Tinted Drytouch NT ndc-match (0.95)

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"}