Mineral Sunscreen Non-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 Sunscreen Non-Tinted
Generic name: TITANIUM DIOXIDE, ZINC OXIDE
Manufacturer: LOTUS SKINCARE AND MAKE-UP STUDIO
Product type: HUMAN OTC DRUG
SPL set ID: 36b000e3-2516-932c-e063-6294a90a0e41
SPL ID: 46285cb3-d24d-0451-e063-6394a90a0fe3
Version: 2
Effective date: 2025-12-17
Source export date: 2026-10-27
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 21:01:21

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 Sunscreen Non-Tinted	openfda.brand_name
generic name		TITANIUM DIOXIDE, ZINC OXIDE	openfda.generic_name
manufacturer name		LOTUS SKINCARE AND MAKE-UP STUDIO	openfda.manufacturer_name
ndc	package	85558-202-50	openfda.package_ndc
ndc	product	85558-202	openfda.product_ndc
ndc11	package	85558020250	derived:openfda.package_ndc
spl id		46285cb3-d24d-0451-e063-6394a90a0fe3	id
spl set id		36b000e3-2516-932c-e063-6294a90a0e41	set_id
unii		SOI2LOH54Z	openfda.unii
unii		15FIX9V2JP	openfda.unii

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