KIEHLS SINCE 1851 BODY FUEL ANTIPERSPIRANT AND DEODORANT- aluminum chlorohydrate lotion

Kiehls Since 1851 Body Fuel Antiperspirant and Deodorant by

Drug Labeling and Warnings

Kiehls Since 1851 Body Fuel Antiperspirant and Deodorant by is a Otc medication manufactured, distributed, or labeled by L'Oreal USA Products Inc, Fareva Richmond, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Aluminum chlorohydrate 12%

Purpose

Antiperspirant

Use

reduces underarm wetness

Warnings

For external use only

Do not use

on broken skin

Stop use if

rash or irritation occurs

Ask a doctor before use if

you have kidney disease

Keep out of reach of children.

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

Directions

apply to underarms only

Inactive ingredients

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

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KIEHLS SINCE 1851 BODY FUEL ANTIPERSPIRANT AND DEODORANT 
aluminum chlorohydrate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-639
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	120 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETEARETH-33 (UNII: R42C2O714B)
PERLITE (UNII: 0SG101ZGK9)
DIMETHICONE (UNII: 92RU3N3Y1O)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
CAFFEINE (UNII: 3G6A5W338E)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
CITRAL (UNII: T7EU0O9VPP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-639-01	1 in 1 CARTON	03/28/2018
1		75 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	03/28/2018

Labeler - L'Oreal USA Products Inc (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
Fareva Richmond, Inc.		969523245	manufacture(49967-639)