Label: DEODORANT ANTIPERSPIRANT SPRAYS- aluminum chlorohydrate spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated February 3, 2021

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  • SPL UNCLASSIFIED SECTION

    DEODORANT ANTIPERSPIRANT SPRAYS

  • Active Ingredient(s)

    ALUMINUM CHLOROHYDRATE 3g/100mL.

  • Purpose

    Antiperspirant

  • Use

    Reduces underarm wetness.

  • Warnings

    For external use only.

  • Do not use

    • on open skin wounds
  • WHEN USING

    When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • STOP USE

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

  • 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.

  • Directions

    Gently shake several times before using. 15cm away from the skin, evenly sprayed in the armpit or other sweating parts.

  • Other information

    • Store no more than 50℃
  • Inactive ingredients

    o-CYMEN-5-OL
    PROPANE
    BUTANE
    ALCOHOL
    PROPYLENE GLYCOL
    CITRONELLOL
    COUMARIN
    HYDROXYCITRONELLAL
    ISOBUTANE
    GLYCYRRHIZA URALENSIS (LICORICE) ROOT EXTRACT
    PERILLA OCYMOIDES SEED EXTRACT
    HELIANTHUS ANNUUS (SUNFLOWER) FLOWER EXTRACT

  • Package Label - Principal Display Panel

    label

  • INGREDIENTS AND APPEARANCE
    DEODORANT ANTIPERSPIRANT SPRAYS 
    aluminum chlorohydrate spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81531-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ISOBUTANE (UNII: BXR49TP611)  
    O-CYMEN-5-OL (UNII: H41B6Q1I9L)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    GLYCYRRHIZA URALENSIS ROOT (UNII: 42B5YD8F0K)  
    BUTANE (UNII: 6LV4FOR43R)  
    ALCOHOL (UNII: 3K9958V90M)  
    PROPANE (UNII: T75W9911L6)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)  
    COUMARIN (UNII: A4VZ22K1WT)  
    PERILLA FRUTESCENS SEED (UNII: 8M62PUD356)  
    HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81531-101-01100 mL in 1 BOTTLE; Type 0: Not a Combination Product02/04/2021
    2NDC:81531-101-02120 mL in 1 BOTTLE; Type 0: Not a Combination Product02/04/2021
    3NDC:81531-101-03150 mL in 1 BOTTLE; Type 0: Not a Combination Product02/04/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35002/04/2021
    Labeler - Guangzhou Ronghui Cosmetics Co., Ltd. (553638678)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Ronghui Cosmetics Co., Ltd.553638678manufacture(81531-101)
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