Alumier MD Moisture Matte Broad Spectrum SPF 40 Sunscreen Amber

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: Alumier MD Moisture Matte Broad Spectrum SPF 40 Sunscreen Amber
Generic name: ZINC OXIDE, TITANIUM DIOXIDE
Manufacturer: Alumier Labs
Product type: HUMAN OTC DRUG
SPL set ID: ba864a08-e66d-d286-e053-2995a90a1854
SPL ID: 28689862-f8cc-5f28-e063-6294a90ac654
Version: 5
Effective date: 2024-12-03
Source export date: 2026-10-12
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:29:43

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

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 · 25 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M020	openfda.application_number
brand name		Alumier MD Moisture Matte Broad Spectrum SPF 40 Sunscreen Sand	openfda.brand_name
brand name		Alumier MD Moisture Matte Broad Spectrum SPF 40 Sunscreen Ivory	openfda.brand_name
brand name		Alumier MD Moisture Matte Broad Spectrum SPF 40 Sunscreen Amber	openfda.brand_name
generic name		ZINC OXIDE, TITANIUM DIOXIDE	openfda.generic_name
manufacturer name		Alumier Labs	openfda.manufacturer_name
ndc	package	69473-016-02	openfda.package_ndc
ndc	package	69473-014-01	openfda.package_ndc
ndc	package	69473-016-01	openfda.package_ndc
ndc	package	69473-015-02	openfda.package_ndc
ndc	package	69473-014-02	openfda.package_ndc
ndc	package	69473-015-01	openfda.package_ndc
ndc	product	69473-015	openfda.product_ndc
ndc	product	69473-016	openfda.product_ndc
ndc	product	69473-014	openfda.product_ndc
ndc11	package	69473001502	derived:openfda.package_ndc
ndc11	package	69473001501	derived:openfda.package_ndc
ndc11	package	69473001601	derived:openfda.package_ndc
ndc11	package	69473001401	derived:openfda.package_ndc
ndc11	package	69473001402	derived:openfda.package_ndc
ndc11	package	69473001602	derived:openfda.package_ndc
spl id		28689862-f8cc-5f28-e063-6294a90ac654	id
spl set id		ba864a08-e66d-d286-e053-2995a90a1854	set_id
unii		SOI2LOH54Z	openfda.unii
unii		15FIX9V2JP	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. When using this product do not use on damaged or broken skin keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if you develop severe irritation, burning or itching of the skin, hives, swelling of eyes and mouth, blistering or difficulty breathing. Keep out of reach of children. If swallowed, call a Poison Control Center or get medical help right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.