Label: CHARM TEX 3 IN 1 ANTIBACTERIAL SHAVE GEL BODY WASH- benzethonium chloride lotion/shampoo

  • NDC Code(s): 77573-009-01, 77573-009-02, 77573-009-03, 77573-009-04
  • Packager: Jiangsu Aimeili Cosmetic Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 5, 2024

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  • Active Ingredient

    Benzethonium Chloride 0.1%

  • Purpose

    Antiseptic

  • Use

    As shaving gel: Smooth skin when do shaving and help reduce bacteria

    As body wash: Body cleaning to help reduce bacteria

    As shampoo: Hair cleaning to help reduce bacteria

  • Warnings

    For external use only

  • STOP USE

    Keep out of eyes, ears, and mouth. In case of eye contact, flush eyes with water

    Stop use and ask a doctor if irritation and redness develop or if condition persists for more than 72 hours

  • 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

    As shave gel: Wet skin and squeeze gel onto figer tips. Spread gel evenly on skin and shave

    As body wash: Squeeze body wash onto wet hand or wash cloth.  Apply, lather, and rinse.

    As shampoo: Wet hair, apply shampoo, work up a rich lather and rinse

  • Inactive ingredients

    Water, Cocamidopropyl Betaine, Sodium Lauryl Sulfate, Cocamide Dea, Sodium Chloride, DMDM Hydantoin, Fragrance, Citric Acid

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    CHARM TEX 3 IN 1 ANTIBACTERIAL SHAVE GEL BODY WASH 
    benzethonium chloride lotion/shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77573-009
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE0.1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77573-009-0157 g in 1 BOTTLE; Type 0: Not a Combination Product03/14/2021
    2NDC:77573-009-02118 g in 1 BOTTLE; Type 0: Not a Combination Product03/14/2021
    3NDC:77573-009-03236 g in 1 BOTTLE; Type 0: Not a Combination Product03/14/2021
    4NDC:77573-009-043760 g in 1 BOTTLE; Type 0: Not a Combination Product03/14/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00503/14/2021
    Labeler - Jiangsu Aimeili Cosmetic Co.,Ltd. (543903077)
    Establishment
    NameAddressID/FEIBusiness Operations
    Jiangsu Aimeili Cosmetic Co.,Ltd.543903077manufacture(77573-009)
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