Package 84203-001-01

Brand: sunscreen

Generic: titanium dioxide 6.8%
NDC Package

Package Facts

Identity

Package NDC 84203-001-01
Digits Only 8420300101
Product NDC 84203-001
Product ID 84203-001_3aaee79a-2b7f-1b14-e063-6294a90af5b1
Description

30 mL in 1 TUBE (84203-001-01)

Marketing

Marketing Status
Marketed Since 2024-03-25
Brand sunscreen
Generic titanium dioxide 6.8%
Sample Package No

Linked Drug Pages (1)

Sunscreen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "3aaee79a-2b7f-1b14-e063-6294a90af5b1", "openfda": {"unii": ["15FIX9V2JP"], "spl_set_id": ["146030bc-2bf4-25ea-e063-6294a90a4613"], "manufacturer_name": ["Baxter of California, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 TUBE (84203-001-01)", "package_ndc": "84203-001-01", "marketing_start_date": "20240325"}], "brand_name": "Sunscreen", "product_id": "84203-001_3aaee79a-2b7f-1b14-e063-6294a90af5b1", "dosage_form": "LIQUID", "product_ndc": "84203-001", "generic_name": "Titanium Dioxide 6.8%", "labeler_name": "Baxter of California, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sunscreen", "active_ingredients": [{"name": "TITANIUM DIOXIDE", "strength": ".068 g/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240325", "listing_expiration_date": "20261231"}