Neutrogena Ultra Sheer Dry-Touch Sunscreen MAX Broad Spectrum SPF 100 Plus

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: Neutrogena Ultra Sheer Dry-Touch Sunscreen MAX Broad Spectrum SPF 100 Plus
Generic name: AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Manufacturer: Kenvue Brands LLC
Product type: HUMAN OTC DRUG
SPL set ID: 3bac8d0a-8726-46c3-e063-6294a90a1075
SPL ID: 3bac8c1d-38f4-122c-e063-6394a90af040
Version: 1
Effective date: 2025-08-06
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 02:56:21

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		Neutrogena Ultra Sheer Dry-Touch Sunscreen MAX Broad Spectrum SPF 100 Plus	openfda.brand_name
generic name		AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	openfda.generic_name
manufacturer name		Kenvue Brands LLC	openfda.manufacturer_name
ndc	package	69968-0936-1	openfda.package_ndc
ndc	package	69968-0936-3	openfda.package_ndc
ndc	product	69968-0936	openfda.product_ndc
ndc11	package	69968093603	derived:openfda.package_ndc
ndc11	package	69968093601	derived:openfda.package_ndc
spl id		3bac8c1d-38f4-122c-e063-6394a90af040	id
spl set id		3bac8d0a-8726-46c3-e063-6294a90a1075	set_id
unii		5A68WGF6WM	openfda.unii
unii		V06SV4M95S	openfda.unii
unii		G63QQF2NOX	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 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, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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