YOUTH DEW ROLL-ON ANTIPERSPIRANT DEODORANT- aluminum chlorohydrate liquid

YOUTH DEW ROLL-ON ANTIPERSPIRANT DEODORANT by

Drug Labeling and Warnings

YOUTH DEW ROLL-ON ANTIPERSPIRANT DEODORANT by is a Otc medication manufactured, distributed, or labeled by ESTEE LAUDER INC, Estee Lauder Companies Inc., PALC, Estee Lauder Cosmetics Ltd., Whitman Laboratories Ltd., Estee Lauder N.V., The Estee Lauder Inc, Northtec LLC, PADC 1. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENT:ALUMINUM CHLOROHYDRATE 20.00%

PURPOSE

USES: DECREASES UNDERARM PERSPIRATION

WARNINGS

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.

DOSAGE & ADMINISTRATION

DIRECTIONS: APPLY TO UNDERARMS ONLY

INACTIVE INGREDIENT

INACTIVE INGREDIENTS: WATER [] STEARETH-2 [] ALCOHOL DENAT. [] PPG-11 STEARYL ETHER [] STEARETH-20 [] YOUTH-DEW FRAGRANCE (PARFUM) [] MYRISTALKONIUM CHLORIDE [] QUATERNIUM-14 []TRISODIUM EDTA [] SORBIC ACID ILN32521

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL:

YOUTH-DEW

ROLL-ON
ANTI-PERSPIRANT
DEODORANT

ACTIVE INGREDIENT: ALUMINUM CHLOROHYDRATE 20.00%

2.5 FL OZ LIQ/ 75 mL

ESTEE LAUDER DIST

NY, NY 10022

INGREDIENTS AND APPEARANCE

YOUTH DEW ROLL-ON ANTIPERSPIRANT DEODORANT 
aluminum chlorohydrate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11559-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (aluminum cation - UNII:3XHB1D032B)	ALUMINUM CHLOROHYDRATE	20 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11559-001-01	75 mL in 1 BOTTLE, WITH APPLICATOR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	04/01/1977

Labeler - ESTEE LAUDER INC (005914387)

Establishment
Name	Address	ID/FEI	Business Operations
ESTEE LAUDER COSMETICS, LTD		205952385	manufacture

Establishment
Name	Address	ID/FEI	Business Operations
ESTEE LAUDER N.V.		370151326	manufacture

Establishment
Name	Address	ID/FEI	Business Operations
Len-Ron Manufacturing Division of Aramis Inc.		809771152	manufacture

Establishment
Name	Address	ID/FEI	Business Operations
Aramis Inc.		042918826	manufacture

Establishment
Name	Address	ID/FEI	Business Operations
Northtec Bristol		949264774	manufacture, relabel, repack

Establishment
Name	Address	ID/FEI	Business Operations
Northtec Keystone		618107429	manufacture, relabel, repack

Establishment
Name	Address	ID/FEI	Business Operations
PADC 1		110482184	manufacture, relabel, repack

Establishment
Name	Address	ID/FEI	Business Operations
Estee Lauder Pennsylvania Distribution Center 2		828534516	manufacture, relabel, repack

Establishment
Name	Address	ID/FEI	Business Operations
Estee Lauder Cosmetics, Ltd.		255175580	manufacture

Establishment
Name	Address	ID/FEI	Business Operations
Estee Lauder Cosmetics, Ltd		253616536	manufacture

Establishment
Name	Address	ID/FEI	Business Operations
Estee Lauder Cosmetics Distribution Center		208579636	manufacture, label, relabel

Establishment
Name	Address	ID/FEI	Business Operations
Estee Lauder Kabushiki Kaisha		712808195	relabel, repack

Establishment
Name	Address	ID/FEI	Business Operations
Whitman Laboratories Ltd.		216866277	manufacture

Establishment
Name	Address	ID/FEI	Business Operations
Aveda Corporation		071352058	manufacture