Kiehls Since 1851 Body Fuel Antiperspirant and Deodorant

Manufacturer
L'Oreal USA Products Inc | Fareva Richmond, Inc.
Effective date
2023-12-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:06:10

Label at a glance#

ProductKiehls Since 1851 Body Fuel Antiperspirant and Deodorant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure12 sections

Dosage and administration

apply to underarms only

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum chlorohydrate 12%

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, cetearyl alcohol, fragrance, ceteareth-33, perlite, dimethicone, phenoxyethanol, pentylene glycol, limonene, caffeine, tocopheryl acetate, zinc gluconate, ascorbyl glucoside, linalool, citral

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7dea7767-9f52-b60a-5435-33cb9cc28baeProduct name420250124
6338270f-96cb-0ecb-6fbb-0a9bc78001f4Product name720250116
0ca83774-3f79-b837-5d6f-c210102f3bc8Product name620250114
41b814f3-0166-1c53-c9ef-a0794c7daf9dProduct name320221110
a590be26-846c-8659-a5a1-fb25907965dcProduct name220221110
2dc76302-91c0-4c35-ad78-99adfb049c4bProduct name120200603
e6065d4b-5ae1-476f-a40e-f2851cbb5d2bProduct name220180221
f212291f-05fe-9603-fc7e-bd73e38ce1e6Product name220161129
182f9ab4-4ab5-c449-200f-87ce2ce8e550Product name220151105
332e86c3-7875-ca6e-f934-2206d2b31996Product name120140508
56625fcc-aa34-9d30-d0e9-1c1beb37ea21Product name120140508
7dfac40f-a405-cd2e-7c06-3059ec0e1092Product name120140508
96c2be53-8e44-452d-56a2-d255b2f1af2dProduct name120140508
bf8bd5f7-495f-4022-2780-7ded7ea7ea44Product name120140508
d223c173-c39b-d764-47d4-d671d3088815Product name120140508
e01133ad-4dcd-c7f3-454b-2ff569ee160aProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49967-639-01Kiehls Since 1851 Body Fuel Antiperspirant and Deodorant75 mL in 1 BOTTLE, WITH APPLICATORLOTION753
49967-639-01Kiehls Since 1851 Body Fuel Antiperspirant and Deodorant1 in 1 CARTONLOTION13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49967-639KIEHLS SINCE 1851 BODY FUEL ANTIPERSPIRANT AND DEODORANT (ALUMINUM CHLOROHYDRATE) LOTION [L'OREAL USA PRODUCTS INC]3Current NDC, Legacy NDC, 2 package rows20231231_f5ef03e1-aa3b-4cc5-8734-7b912daf0c79.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-63949967-639-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

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 Body Fuel Antiperspirant and DeodorantALUMINUM CHLOROHYDRATEL'Oreal USA Products Incf5ef03e1-aa3b-4cc5-8734-7b912daf0c792023-12-30WarningsExact identifier
ndc (package): 49967-639-01
ndc (product): 49967-639
ndc11 (package): 49967063901
spl id: 9b92a444-cab4-4c29-a0cc-2e052079380f
spl set id: f5ef03e1-aa3b-4cc5-8734-7b912daf0c79

Reported adverse events (FAERS/openFDA)#

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