Package 85334-203-15

Brand: matte velvet tint

Generic: titanium dioxide, zinc oxide
NDC Package Sample

Package Facts

Identity

Package NDC 85334-203-15
Digits Only 8533420315
Product NDC 85334-203
Product ID 85334-203_45c8d06e-3608-6de7-e063-6294a90adee5
Description

1.5 g in 1 PACKET (85334-203-15)

Marketing

Marketing Status
Marketed Since 2024-04-19
Brand matte velvet tint
Generic titanium dioxide, zinc oxide
Sample Package Yes

Linked Drug Pages (1)

Matte Velvet Tint ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "45c8d06e-3608-6de7-e063-6294a90adee5", "openfda": {"unii": ["15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["359641c5-0e19-f243-e063-6394a90aeebc"], "manufacturer_name": ["Brent Loftis, D.O., Inc., A California Medical Corporation"]}, "finished": true, "packaging": [{"sample": true, "description": "1.5 g in 1 PACKET (85334-203-15)", "package_ndc": "85334-203-15", "marketing_start_date": "20240419"}], "brand_name": "Matte Velvet Tint", "product_id": "85334-203_45c8d06e-3608-6de7-e063-6294a90adee5", "dosage_form": "CREAM", "product_ndc": "85334-203", "generic_name": "Titanium Dioxide, Zinc Oxide", "labeler_name": "Brent Loftis, D.O., Inc., A California Medical Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Matte Velvet Tint", "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": "20240419", "listing_expiration_date": "20261231"}