Label: MEMBERS SELECTION ANTIBACTERIAL- benzalkonium chloride liquid

  • 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, 2015

If you are a consumer or patient please visit this version.

View All Sections
  • Active ingredient / Ingrediente activo

    Benzalkonium Chloride 0.10%

    Purpose / Propósito

    Antibacterial / Antibacteriano

  • Uses / Usos

    For washing to decrease bacteria on the skin. / Para lavar y disminuir las bacterias en la piel

  • Warnings / Advertencias

    For external use only / Solo para uso externo

    When using this product / Al usar este producto

    avoid contact with eyes. If contact occurs, rinse thoroughly with water. / evitar el contacto con los ojos. Si ocurriera, enjuagar bien con agua.

    Stop use and ask a doctor if / Interrumpir el uso y consultar a un médico si

    irritation and redness develops. / se product irritación y enrojecimiento

    Keep out of reach of children. / Mantenga fuera del alcance de los niños.

    In case of poisoning, seek medical attention and provide this package. Call the National Poison Centers / En caso de intoxicación consulte al médico y aporte esta etiqueta. Para llamar al Centro Nacional de Intoxicaciones: Panama 911; Costa Rica (506) 2223-1028, Emergency/Emergencias 911; Guatemala (502) 2251-3560; Nicaragua (505) 2289-7150; El Salvador (503) 2288-0417; Honduras (504) 2232-2322

  • Directions / Instrucciones

    • Apply onto wet hands / Aplicar en las manos húmedas
    • Work into rich later and rinse off / Formar espuma y enjuagar bien
  • Other Information

    Store at room temperature / Guardar a temperatura ambiente

  • Inactive ingredients / Ingredientes inactivos

    Water (Aqua), Cocamidopropyl Betaine, Glycerin, Decyl Glucosid, Hydroxyethylcellulose, Aloe Barbadensis Leaf Juice, Fragrance (Parfum), Poloxamer 124, Polyquaternium-7, Tetrasodium EDTA, Citric Acid, Sodium Citrate, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090), Red 33 (CI 17200).

    Agua (Aqua), Cocamidopropil betaína, glicerina, decil glucósido, hidroxietil celulosa, jugo de hoja de aloe barbadensis, fragrancia (parfume), poloxamer 124, policuaternio 7, EDTA tetrasódico, ácido cítrico, citrato de sodio, meticloroisotiazolinona, metilisotiasolinona, azul (CI 42090), rojo (CI 17200)

  • Label Copy

    Image of the label

  • INGREDIENTS AND APPEARANCE
    MEMBERS SELECTION ANTIBACTERIAL 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63148-079
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    POLOXAMER 124 (UNII: 1S66E28KXA)  
    POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63148-079-802360 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E08/09/2015
    Labeler - APOLLO HEALTH AND BEAUTY CARE (201901209)
    Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    APOLLO HEALTH AND BEAUTY CARE201901209manufacture(63148-079)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!