ULTRA VIOLETTE Unblock Screen 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: ULTRA VIOLETTE Unblock Screen SPF 50 Sunscreen
Generic name: BEMOTRIZINOL, OCTOCRYLENE, ZINC OXIDE
Manufacturer: Grace and Fire USA Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 56ad0dce-410e-9d78-e063-6294a90a1c3e
SPL ID: 56ad0dce-410f-9d78-e063-6294a90a1c3e
Version: 1
Effective date: 2026-08-09
Source export date: 2026-10-12
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/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:57:12

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M020	openfda.application_number
brand name		ULTRA VIOLETTE Unblock Screen SPF 50 Sunscreen	openfda.brand_name
generic name		BEMOTRIZINOL, OCTOCRYLENE, ZINC OXIDE	openfda.generic_name
manufacturer name		Grace and Fire USA Inc.	openfda.manufacturer_name
ndc	package	84803-116-50	openfda.package_ndc
ndc	package	84803-116-05	openfda.package_ndc
ndc	product	84803-116	openfda.product_ndc
ndc11	package	84803011605	derived:openfda.package_ndc
ndc11	package	84803011650	derived:openfda.package_ndc
spl id		56ad0dce-410f-9d78-e063-6294a90a1c3e	id
spl set id		56ad0dce-410e-9d78-e063-6294a90a1c3e	set_id
unii		5A68WGF6WM	openfda.unii
unii		SOI2LOH54Z	openfda.unii
unii		PWZ1720CBH	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. Do not use on damaged or broken skin When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs 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.