Label: YOUTH DEW ROLL-ON ANTIPERSPIRANT DEODORANT- aluminum chlorohydrate liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 22, 2023

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  • ACTIVE INGREDIENT

    ACTIVE INGREDIENT: ALUMINUM CHLOROHYDRATE 20.00%

  • INDICATIONS & USAGE

    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 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
  • INGREDIENTS AND APPEARANCE
    YOUTH DEW ROLL-ON ANTIPERSPIRANT DEODORANT 
    aluminum chlorohydrate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11559-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE200 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    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)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11559-001-0175 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product12/02/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01912/02/2020
    Labeler - ESTEE LAUDER INC (005914387)
    Registrant - Estee Lauder Companies Inc. (790802086)
    Establishment
    NameAddressID/FEIBusiness Operations
    Whitman Laboratories Ltd.216866277manufacture(11559-001) , pack(11559-001) , label(11559-001)
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