Label: SKIN AID MEDICS ANTIBACTERIAL COCONUT GINGER- benzalkonium chloride 0.13% gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 August 10, 2020

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  • Active Ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antibacterial

  • Uses

    For handwashing to decrease bacteria on the skin

  • Warnings

    For external use only.

  • When using this product

    When using this product. Avoid contact with eyes. In case of eye contact, rinse eyes thoroughly with water.

  • Stop use and ask a doctor

    Stop use and ask a doctor if irritation or redness develops.

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center immediately.

  • Directions

    Pump into hands, wet as needed. Lather vigorously for at least 20 seconds. Wash skin, rinse thoroughly and dry.

  • Other Information

    -Store between 15-30C (59-86F).

    -Avoid freezing and excessive heat above 40C (104F)

  • Inactive Ingredients

    Aqua Water, sodium laureth sulfate, cocoamidopropyl betaine, sodium chloride, glycerin, parfum, PEG-150 Distearate, Aloe Barbadensis Leaf Juice, Disodium EDTA, Methylchloroisothiazolinone, Methylisothazolinone, magnesium chloride, Magnesium Nitrate, Citric Acid, Tocopheryl Acetate

  • Skin-aid-medics Antibacterial Hand Soap Coconut Ginger

    label

  • INGREDIENTS AND APPEARANCE
    SKIN AID MEDICS ANTIBACTERIAL COCONUT GINGER 
    benzalkonium chloride 0.13% gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73166-106
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.65 g  in 500 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
    MAGNESIUM CHLORIDE ANHYDROUS (UNII: 59XN63C8VM)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYETHYLENE GLYCOL 100000 (UNII: V46Y6OJ5QB)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    WATER (UNII: 059QF0KO0R)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    DISODIUM EDTA-COPPER (UNII: 6V475AX06U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73166-106-16500 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/01/2020
    Labeler - Larry (Xiamen) Hi Tech Co., Ltd (529759328)
    Registrant - G2 Beauty Inc (124608169)
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