Package 85331-208-50

Brand: tinted sunscreen

Generic: zinc oxide
NDC Package

Package Facts

Identity

Package NDC 85331-208-50
Digits Only 8533120850
Product NDC 85331-208
Description

53 g in 1 BOTTLE, PUMP (85331-208-50)

Marketing

Marketing Status
Marketed Since 2022-07-20
Brand tinted sunscreen
Generic zinc oxide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "45af1972-d2cc-1b3f-e063-6394a90a88dd", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["34a54441-c741-0c46-e063-6294a90a9be8"], "manufacturer_name": ["Scottsdale Skin Boutique and Dermatology Pllc"]}, "finished": true, "packaging": [{"sample": false, "description": "53 g in 1 BOTTLE, PUMP (85331-208-50)", "package_ndc": "85331-208-50", "marketing_start_date": "20220720"}], "brand_name": "Tinted Sunscreen", "product_id": "85331-208_45af1972-d2cc-1b3f-e063-6394a90a88dd", "dosage_form": "CREAM", "product_ndc": "85331-208", "generic_name": "Zinc Oxide", "labeler_name": "Scottsdale Skin Boutique and Dermatology Pllc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tinted Sunscreen", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "160 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220720", "listing_expiration_date": "20261231"}