Blue Lizard Sensitive 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 Sensitive Sunscreen
Generic name: TITANIUM DIOXIDE AND ZINC OXIDE
Manufacturer: Crown Laboratories
Product type: HUMAN OTC DRUG
SPL set ID: 1e4d49f4-9e77-48b5-bce5-ff04ed885a0f
SPL ID: 48345730-de18-7fb2-e063-6394a90a9b5d
Version: 19
Effective date: 2026-01-12
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:57:13

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M020	openfda.application_number
brand name		Blue Lizard Sensitive Sunscreen	openfda.brand_name
generic name		TITANIUM DIOXIDE AND ZINC OXIDE	openfda.generic_name
manufacturer name		Crown Laboratories	openfda.manufacturer_name
ndc	package	0316-2045-60	openfda.package_ndc
ndc	package	0316-2045-10	openfda.package_ndc
ndc	package	0316-2045-40	openfda.package_ndc
ndc	package	0316-2045-45	openfda.package_ndc
ndc	package	0316-2045-30	openfda.package_ndc
ndc	package	0316-2045-50	openfda.package_ndc
ndc	product	0316-2045	openfda.product_ndc
ndc11	package	00316204510	derived:openfda.package_ndc
ndc11	package	00316204540	derived:openfda.package_ndc
ndc11	package	00316204560	derived:openfda.package_ndc
ndc11	package	00316204530	derived:openfda.package_ndc
ndc11	package	00316204545	derived:openfda.package_ndc
ndc11	package	00316204550	derived:openfda.package_ndc
spl id		48345730-de18-7fb2-e063-6394a90a9b5d	id
spl set id		1e4d49f4-9e77-48b5-bce5-ff04ed885a0f	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 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.