MOISTURE SURGE SPF

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: MOISTURE SURGE SPF
Generic name: AVOBENZONE,HOMOSALATE,OCTINOXATE,OCTISALATE
Manufacturer: CLINIQUE LABORATORIES LLC
Product type: HUMAN OTC DRUG
SPL set ID: ec921e21-db68-db77-e053-2a95a90a5781
SPL ID: 3c69d84d-44cd-2449-e063-6294a90afa4c
Version: 7
Effective date: 2025-08-15
Source export date: 2026-10-27
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/55ffdfed5c29f1b4aed512886bd3fb7831e157cc4948137779971a558752ed2b/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:07:24

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 · 23 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M020	openfda.application_number
brand name		MOISTURE SURGE SPF	openfda.brand_name
generic name		AVOBENZONE,HOMOSALATE,OCTINOXATE,OCTISALATE	openfda.generic_name
manufacturer name		CLINIQUE LABORATORIES LLC	openfda.manufacturer_name
ndc	package	49527-084-01	openfda.package_ndc
ndc	package	49527-084-05	openfda.package_ndc
ndc	package	49527-084-04	openfda.package_ndc
ndc	package	49527-084-06	openfda.package_ndc
ndc	package	49527-084-02	openfda.package_ndc
ndc	package	49527-084-03	openfda.package_ndc
ndc	product	49527-084	openfda.product_ndc
ndc11	package	49527008402	derived:openfda.package_ndc
ndc11	package	49527008404	derived:openfda.package_ndc
ndc11	package	49527008401	derived:openfda.package_ndc
ndc11	package	49527008403	derived:openfda.package_ndc
ndc11	package	49527008405	derived:openfda.package_ndc
ndc11	package	49527008406	derived:openfda.package_ndc
spl id		3c69d84d-44cd-2449-e063-6294a90afa4c	id
spl set id		ec921e21-db68-db77-e053-2a95a90a5781	set_id
unii		V06SV4M95S	openfda.unii
unii		G63QQF2NOX	openfda.unii
unii		4X49Y0596W	openfda.unii
unii		4Y5P7MUD51	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 WARNINGS 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 product is 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.