Blue Lizard Sport SPF 50 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: Blue Lizard Sport SPF 50 Sunscreen
Generic name: OCTISALATE AND TITANIUM DIOXIDE AND ZINC OXIDE
Manufacturer: Crown Laboratories
Product type: HUMAN OTC DRUG
SPL set ID: 4955fa1c-789d-4f42-af75-70223310644a
SPL ID: 50c4e0bf-354b-c1d1-e063-6394a90a8fee
Version: 8
Effective date: 2026-05-01
Source export date: 2026-10-30
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/2026-10-30/9dea423b9e87a781c152bc6e136923fb91acb0732a7a0ec0d2a51142148f160c/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:43:23

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M020	openfda.application_number
brand name		Blue Lizard Sport SPF 50 Sunscreen	openfda.brand_name
generic name		OCTISALATE AND TITANIUM DIOXIDE AND ZINC OXIDE	openfda.generic_name
manufacturer name		Crown Laboratories	openfda.manufacturer_name
ndc	package	0316-2075-45	openfda.package_ndc
ndc	package	0316-2075-30	openfda.package_ndc
ndc	package	0316-2075-50	openfda.package_ndc
ndc	package	0316-2075-40	openfda.package_ndc
ndc	product	0316-2075	openfda.product_ndc
ndc11	package	00316207545	derived:openfda.package_ndc
ndc11	package	00316207550	derived:openfda.package_ndc
ndc11	package	00316207530	derived:openfda.package_ndc
ndc11	package	00316207540	derived:openfda.package_ndc
spl id		50c4e0bf-354b-c1d1-e063-6394a90a8fee	id
spl set id		4955fa1c-789d-4f42-af75-70223310644a	set_id
unii		SOI2LOH54Z	openfda.unii
unii		15FIX9V2JP	openfda.unii
unii		4X49Y0596W	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 • When using this product • Keep out of eyes. Rinse with water to remove • Stop use and ask doctor if • Rash or irritation occurs • Do not use • On damaged or broken skin • If allergic to any ingredient • If swallowed, get medical help or contact a Poison Control Center

Reported adverse events (FAERS/openFDA)#

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