Package 84271-001-01

Brand: seytu body sunscreen

Generic: titanium dioxide and zinc oxide
NDC Package

Package Facts

Identity

Package NDC 84271-001-01
Digits Only 8427100101
Product NDC 84271-001
Product ID 84271-001_1959d76a-87e7-4cdd-9f18-40635e23e2a7
Description

1 TUBE in 1 BOX (84271-001-01) / 120 mL in 1 TUBE

Marketing

Marketing Status
Marketed Since 2024-04-15
Brand seytu body sunscreen
Generic titanium dioxide and zinc oxide
Sample Package No

Linked Drug Pages (1)

SEYTU Body Sunscreen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "1959d76a-87e7-4cdd-9f18-40635e23e2a7", "openfda": {"unii": ["15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["c411e9a6-b2ea-446b-a886-b92c61736e6c"], "manufacturer_name": ["Omnilife USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (84271-001-01)  / 120 mL in 1 TUBE", "package_ndc": "84271-001-01", "marketing_start_date": "20240415"}], "brand_name": "SEYTU Body Sunscreen", "product_id": "84271-001_1959d76a-87e7-4cdd-9f18-40635e23e2a7", "dosage_form": "CREAM", "product_ndc": "84271-001", "generic_name": "titanium dioxide and zinc oxide", "labeler_name": "Omnilife USA, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SEYTU Body Sunscreen", "active_ingredients": [{"name": "TITANIUM DIOXIDE", "strength": "8.3 g/100mL"}, {"name": "ZINC OXIDE", "strength": "4.875 g/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240415", "listing_expiration_date": "20271231"}