Non-Tinted Mineral Foaming Sunscreen

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: Non-Tinted Mineral Foaming Sunscreen
Generic name: TITANIUM DIOXIDE, ZINC OXIDE
Manufacturer: Restore Skin Therapy, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 364b6af2-a0ed-4a17-e063-6394a90a3a17
SPL ID: 459bfcc2-12be-82a9-e063-6294a90a6ca3
Version: 2
Effective date: 2025-12-10
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:19:34

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		Non-Tinted Mineral Foaming Sunscreen	openfda.brand_name
generic name		TITANIUM DIOXIDE, ZINC OXIDE	openfda.generic_name
manufacturer name		Restore Skin Therapy, LLC	openfda.manufacturer_name
ndc	package	85313-211-04	openfda.package_ndc
ndc	product	85313-211	openfda.product_ndc
ndc11	package	85313021104	derived:openfda.package_ndc
spl id		459bfcc2-12be-82a9-e063-6294a90a6ca3	id
spl set id		364b6af2-a0ed-4a17-e063-6394a90a3a17	set_id
unii		SOI2LOH54Z	openfda.unii
unii		15FIX9V2JP	openfda.unii

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