ACTIVE INGREDIENT: ALUMINUM CHLOROHYDRATE 20.00%

USES: DECREASES UNDERARM PERSPIRATION

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\aqua\eau•steareth-2•alcohol denat.•ppg-11 stearyl ether•steareth-20•youth-dew fragrance (parfum)•myristalkonium chloride•quaternium-14•benzyl salicylate•linalool•hydroxycitronellal•geraniol•citronellol•eugenol•limonene•cinnamyl alcohol•coumarin•hexyl cinnamal•trisodium edta•sorbic acid <iln37908>

PRINCIPAL DISPLAY PANEL - 75 ml Bottle Label

YOUTH-DEW

Roll-On
Anti-Perspirant Deodorant

Active Ingredient:
Aluminum Chlorohydrate 20%

2.5 FL. OZ. LIQ. /75ml ℮

ESTĒE LAUDER

PRINCIPAL DISPLAY PANEL - 75 ml Bottle Label

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

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	200 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
LINALOOL, (+)- (UNII: F4VNO44C09)
HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
GERANIOL (UNII: L837108USY)
CITRONELLOL ACETATE, (R)- (UNII: 9X45FJL446)
EUGENOL (UNII: 3T8H1794QW)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
CINNAMYL ALCOHOL (UNII: SS8YOP444F)
COUMARIN (UNII: A4VZ22K1WT)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
EDETATE TRISODIUM (UNII: 420IP921MB)
SORBIC ACID (UNII: X045WJ989B)
WATER (UNII: 059QF0KO0R)
STEARETH-2 (UNII: V56DFE46J5)
ALCOHOL (UNII: 3K9958V90M)
POLYPROPYLENE GLYCOL 11 STEARYL ETHER (UNII: S4G2J0Y0LG)
STEARETH-20 (UNII: L0Q8IK9E08)
FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)
MYRISTALKONIUM CHLORIDE (UNII: 0W255OL75T)
QUATERNIUM-14 (UNII: ZGE94G6AGI)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:11559-001-01	75 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	12/02/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M019	12/02/2020

Labeler - ESTEE LAUDER INC (005914387)

Registrant - Estee Lauder Companies Inc. (790802086)

Name	Address	ID/FEI	Business Operations
Establishment
Whitman Laboratories Ltd.		216866277	manufacture(11559-001) , pack(11559-001) , label(11559-001)