FDA.reportPublic FDA data

Kiehls Since 1851 Superbly Efficient Antiperspirant and Deodorant

Manufacturer
L'Oreal USA Products Inc | L'OREAL USA, INC.
Effective date
2023-12-30
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:06:04

Label at a glance#

ProductKiehls Since 1851 Superbly Efficient Antiperspirant and Deodorant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure11 sections

Dosage and administration

apply to underarms only

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum chlorohydrate 12.8%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

reduces underarm wetness

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

on broken skin

Stop use if

OTC - STOP USE SECTION

rash or irritation occurs

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

you have kidney disease

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

apply to underarms only

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, isopropyl myristate, cetyl esters, propylene glycol, PEG-75 stearate, glyceryl stearate, cetyl alcohol, ceteth-20, phenoxyethanol, steareth-20, dimethicone, caprylyl glycol, bisabolol, citrus medica limonum (lemon) fruit extract, hamamelis virginiana (witch hazel) water, hydrolyzed linseed extract, citrus aurantium amara (bitter orange) flower extract, farnesol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49967-882-01Kiehls Since 1851 Superbly Efficient Antiperspirant and Deodorant75 mL in 1 TUBECREAM754
49967-882-02Kiehls Since 1851 Superbly Efficient Antiperspirant and Deodorant50 mL in 1 TUBECREAM504

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49967-882KIEHLS SINCE 1851 SUPERBLY EFFICIENT ANTIPERSPIRANT AND DEODORANT (ALUMINUM CHLOROHYDRATE) CREAM [L'OREAL USA PRODUCTS INC]4Current NDC, Legacy NDC, 2 package rows20231231_1252c6dc-c2d5-49b4-9f2a-34c096ee110c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALUMINUM CHLOROHYDRATEACTIVE INGREDIENTHPN8MZW13M1
ALUMINUM CHLOROHYDRATEACTIVE MOIETYHPN8MZW13M1

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-88249967-882-01, 49967-882-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
WATER059QF0KO0RIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
CETYL ESTERS WAXD072FFP9GUIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PEG-75 STEARATEOT38R0N74HIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
CETYL ALCOHOL936JST6JCNIACT
CETETH-20I835H2IHHXIACT
PHENOXYETHANOLHIE492ZZ3TIACT
STEARETH-20L0Q8IK9E08IACT
DIMETHICONE92RU3N3Y1OIACT
CAPRYLYL GLYCOL00YIU5438UIACT
LEVOMENOL24WE03BX2TIACT
LEMON24RS0A988OIACT
HAMAMELIS VIRGINIANA TOP WATERNT00Y05A2VIACT
CITRUS AURANTIUM FLOWERO730ZX2Z83IACT
FARNESOLEB41QIU6JLIACT

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
Kiehls Since 1851 Superbly Efficient Antiperspirant and DeodorantALUMINUM CHLOROHYDRATEL'Oreal USA Products Inc1252c6dc-c2d5-49b4-9f2a-34c096ee110c2023-12-30WarningsExact identifier
ndc (package): 49967-882-01
ndc (package): 49967-882-02
ndc (product): 49967-882
ndc11 (package): 49967088201
ndc11 (package): 49967088202
spl id: dc743499-66e9-46fc-a10e-4958b258afed
spl set id: 1252c6dc-c2d5-49b4-9f2a-34c096ee110c

Reported adverse events (FAERS/openFDA)#

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