ARAMIS LAB SERIES POWER PROTECTOR

Manufacturer
ARAMIS INC | ESTEE LAUDER COSMETICS, LTD | ESTEE LAUDER N.V. | Len-Ron Manufacturing Division of Aramis Inc. | Aramis Inc. | Northtec Bristol | Northtec Keystone | PADC 1 | Estee Lauder Pennsylvania Distribution Center 2 | Estee Lauder Cosmetics, Ltd. | Estee Lauder Cosmetics Distribution Center | Estee Lauder Kabushiki Kaisha | Whitman Laboratories Ltd. | Aveda Corporation
Effective date
2010-04-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:11

Label at a glance#

ProductARAMIS LAB SERIES POWER PROTECTOR SPF 50
Active ingredientOCTISALATE, HOMOSALATE, AVOBENZONE, OXYBENZONE
Label structure3 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION


ACTIVE INGREDIENTS: OCTISALATE 5.00% [] HOMOSALATE 5.00% [] AVOBENZONE 3.00% [] OXYBENZONE 3.00%

WARNINGS SECTION

WARNING: KEEP OUT OF EYES. STOP USE IF IRRITATION OCCURS. KEEP OUT OF REACH OF CHILDREN.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL:

ARAMIS

LAB SERIES
POWER PROTECTOR SPF 50
SKIN CARE FOR MEN


3.4 FL OZ/ 100 ML

ARAMIS INC.
NEW YORK, NY 10022

FOLDING CARTON
FOLDING CARTON

 

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42472-720-012020-01-31C16284748780-19d75b9d0-7912-f424-e053-dadaa90a57cebf79178c-b87c-400d-87c1-9f184f00e12b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42472-720-01ARAMIS LAB SERIES POWER PROTECTORSPF 501 in 1 CARTONLOTION11
42472-720-02ARAMIS LAB SERIES POWER PROTECTORSPF 50100 mL in 1 TUBELOTION1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42472-720ARAMIS LAB SERIES POWER PROTECTOR SPF 50 (OCTISALATE, HOMOSALATE, AVOBENZONE, OXYBENZONE) LOTION [ARAMIS INC]1Legacy NDC, 2 package rows20100407_bf79178c-b87c-400d-87c1-9f184f00e12b.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AVOBENZONEACTIVE INGREDIENTG63QQF2NOX1
HOMOSALATEACTIVE INGREDIENTV06SV4M95S1
OCTISALATEACTIVE INGREDIENT4X49Y0596W1
OXYBENZONEACTIVE INGREDIENT95OOS7VE0Y1
AVOBENZONEACTIVE MOIETYG63QQF2NOX1
HOMOSALATEACTIVE MOIETYV06SV4M95S1
OCTISALATEACTIVE MOIETY4X49Y0596W1
OXYBENZONEACTIVE MOIETY95OOS7VE0Y1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42472-72042472-720-02, 42472-720-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTISALATE4X49Y0596WACTIB
HOMOSALATEV06SV4M95SACTIB
AVOBENZONEG63QQF2NOXACTIB
OXYBENZONE95OOS7VE0YACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c23eb632-a3b9-49ff-b78a-f74c05bfc046bf79178c-b87c-400d-87c1-9f184f00e12b2010-04-06WarningsExact identifier
spl id: c23eb632-a3b9-49ff-b78a-f74c05bfc046
spl set id: bf79178c-b87c-400d-87c1-9f184f00e12b

Reported adverse events (FAERS/openFDA)#

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