Mineral Fusion Tinted

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Mineral Fusion Tinted
Generic name: TITANIUM DIOXIDE, ZINC OXIDE
Manufacturer: FOREFRONT DERMATOLOGY, S.C.
Product type: HUMAN OTC DRUG
SPL set ID: 334ec844-5560-50f7-e063-6394a90a01be
SPL ID: 457632ec-dde4-ba16-e063-6394a90a192a
Version: 2
Effective date: 2025-12-08
Source export date: 2026-09-28
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:12:37

Harmonized routes table
Harmonized routes
TOPICAL

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M020	openfda.application_number
brand name		Mineral Fusion Tinted	openfda.brand_name
generic name		TITANIUM DIOXIDE, ZINC OXIDE	openfda.generic_name
manufacturer name		FOREFRONT DERMATOLOGY, S.C.	openfda.manufacturer_name
ndc	package	85416-203-50	openfda.package_ndc
ndc	product	85416-203	openfda.product_ndc
ndc11	package	85416020350	derived:openfda.package_ndc
spl id		457632ec-dde4-ba16-e063-6394a90a192a	id
spl set id		334ec844-5560-50f7-e063-6394a90a01be	set_id
unii		SOI2LOH54Z	openfda.unii
unii		15FIX9V2JP	openfda.unii

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