La Defense Broad Spectrum SPF 30 Mineral 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: La Defense Broad Spectrum SPF 30 Mineral Sunscreen
Generic name: ZINC OXIDE, TITANIUM DIOXIDE
Manufacturer: Luzern Laboratories, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 3f00befa-415d-415d-89e1-6ba8770ba51e
SPL ID: 3a740766-e09f-b447-e063-6394a90a6c46
Version: 3
Effective date: 2025-07-21
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:26:34

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M020	openfda.application_number
brand name		La Defense Broad Spectrum SPF 30 Mineral Sunscreen	openfda.brand_name
generic name		ZINC OXIDE, TITANIUM DIOXIDE	openfda.generic_name
manufacturer name		Luzern Laboratories, Inc	openfda.manufacturer_name
ndc	package	63127-101-03	openfda.package_ndc
ndc	package	63127-101-01	openfda.package_ndc
ndc	package	63127-101-02	openfda.package_ndc
ndc	product	63127-101	openfda.product_ndc
ndc11	package	63127010103	derived:openfda.package_ndc
ndc11	package	63127010102	derived:openfda.package_ndc
ndc11	package	63127010101	derived:openfda.package_ndc
spl id		3a740766-e09f-b447-e063-6394a90a6c46	id
spl set id		3f00befa-415d-415d-89e1-6ba8770ba51e	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 Avoid contact with eyes. If contact occurs, rinse thoroughly with water. Do not use on damaged or broken skin. Discontinue use if skin irritation develops or increases. If irritation persists, consult a health care practitioner. If swallowed, get medical help or contact a Poison Control Center right away. Keep out of reach of children. Consult a health care practitioner prior to use on children less than six months of age.

Reported adverse events (FAERS/openFDA)#

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