Package 85735-203-50

Brand: clear path tinted facial sunscreen

Generic: titanium dioxide, zinc oxide
NDC Package

Package Facts

Identity

Package NDC 85735-203-50
Digits Only 8573520350
Product NDC 85735-203
Description

53 g in 1 BOTTLE, PUMP (85735-203-50)

Marketing

Marketing Status
Marketed Since 2018-04-24
Brand clear path tinted facial sunscreen
Generic titanium dioxide, zinc oxide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "45782d26-5b24-6cbe-e063-6294a90a4759", "openfda": {"unii": ["15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["37657755-fa82-88a0-e063-6394a90ade47"], "manufacturer_name": ["LULUS SPA BOUTIQUE"]}, "finished": true, "packaging": [{"sample": false, "description": "53 g in 1 BOTTLE, PUMP (85735-203-50)", "package_ndc": "85735-203-50", "marketing_start_date": "20180424"}], "brand_name": "Clear Path Tinted Facial Sunscreen", "product_id": "85735-203_45782d26-5b24-6cbe-e063-6294a90a4759", "dosage_form": "CREAM", "product_ndc": "85735-203", "generic_name": "Titanium Dioxide, Zinc Oxide", "labeler_name": "LULUS SPA BOUTIQUE", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Clear Path Tinted Facial Sunscreen", "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": "20180424", "listing_expiration_date": "20261231"}