sunscreen
Generic: titanium dioxide 6.8%
Labeler: baxter of california, llcDrug Facts
Product Profile
Brand Name
sunscreen
Generic Name
titanium dioxide 6.8%
Labeler
baxter of california, llc
Dosage Form
LIQUID
Routes
Active Ingredients
titanium dioxide .068 g/mL
Manufacturer
Identifiers & Regulatory
Product NDC
84203-001
Product ID
84203-001_3aaee79a-2b7f-1b14-e063-6294a90af5b1
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M020
Listing Expiration
2026-12-31
Marketing Start
2024-03-25
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
84203001
Hyphenated Format
84203-001
Supplemental Identifiers
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
sunscreen (source: ndc)
Generic Name
titanium dioxide 6.8% (source: ndc)
Application Number
M020 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .068 g/mL
Packaging
- 30 mL in 1 TUBE (84203-001-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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"}