KIEHLS CROSSTERRAIN ANTIPERSPIRANT DEODORANT 24 HOUR STRONG DRY- aluminum chlorohydrate stick

Kiehls CrossTerrain Antiperspirant Deodorant by

Drug Labeling and Warnings

Kiehls CrossTerrain Antiperspirant Deodorant by is a Otc medication manufactured, distributed, or labeled by KDC/ONE Development Corporation, Inc, L'Oreal USA Products Inc, Summit Research Labs, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Aluminum Chlorohydrate 20%

Inactive Ingredients

cyclopentasiloxane, mineral oil, stearyl alcohol, hydrogenated castor oil, cetyl alcohol, talc, PEG-100 stearate, glyceryl stearate, fragrance, limonene, lirnalol, benzyl alcohol, citronellol, benzyl salicylate, geraniol, coumarin, citral

Uses Directions

Use reduces underarm wetness

WARNINGS

Warnings

For external use only

Uses

For underarms only

DOSAGE & ADMINISTRATION

Directions apply to underarms only.

ASK DOCTOR

Ask a doctor before use if you have kidney disease.

DO NOT USE

DO NOT USE on broken skin

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KIEHLS CROSSTERRAIN ANTIPERSPIRANT DEODORANT  24 HOUR STRONG DRY
aluminum chlorohydrate stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54565-3901
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	15 g  in 75 g

Inactive Ingredients
Ingredient Name	Strength
TALC (UNII: 7SEV7J4R1U)
PEG-100 STEARATE (UNII: YD01N1999R)
GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
CYCLOMETHICONE (UNII: NMQ347994Z)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
CETYL ALCOHOL (UNII: 936JST6JCN)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
MINERAL OIL (UNII: T5L8T28FGP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54565-3901-1	75 g in 1 CONTAINER; Type 0: Not a Combination Product	10/31/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	10/31/2017

Labeler - Knowlton Development Corporation Inc (204006464)

Establishment
Name	Address	ID/FEI	Business Operations
L'Oreal USA Products Inc		185931458	analysis(54565-3901)

Establishment
Name	Address	ID/FEI	Business Operations
Knowlton Development Corporation Inc		204006464	manufacture(54565-3901) , analysis(54565-3901) , pack(54565-3901) , label(54565-3901)

Establishment
Name	Address	ID/FEI	Business Operations
Summit Research Labs, Inc		825082506	api manufacture(54565-3901)