Label: ANTIMICROBIAL- antimicrobial face and body spray 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 January 22, 2022

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

View All Sections
  • ACTIVE INGREDIENT

    ACTIVE INGREDIENT

    Benzalkonium Chloride 0.13%

  • PURPOSE SECTION

    PURPOSE

    Antiseptic

  • USES

    To help reduce bacteria on the skin

  • WARNINGS

    For external use only

  • When using this product

    *avoid contact with eyes. If eye contact occurs, flush thoroughly with water.

  • Stop use

    Stop use and consult with a doctor. If irritation or redness develops.

  • Keep Out of Reach of Children

    Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

  • Directions

    Directions * Apply a few sprays directly into the face and bodyas often as needed. Allow to dry without wiping. Safe to spray on clothes. Safe to use all day long.

  • Other Information

    Do not store above 104º F.

  • Inactive Ingredients

    Agua (Water),Glycerin, Butylene Glycol, Hyaluronic Acid, Aloe Barbadensis Leaf Juice, Echinacea Purpurea, Sambucus Nigra Fruit, GlycyrrhizaUralensis (Licorice), Origanum Vulgare (Oregano) Leaf, HypericumPerforatum, Uncaria Tomentosa, Polysorbate 20, Citric Acid, Tetrasodium EDTA, Ethylhexylglycerin, Phenoxyethanol, Fragrance.

  • PDP

    MEDILAB

    365

    FACE & BODY SPRAY

    ANTI-BACTERIAL

    ADVANCED HYDRATING FORMULA

    KILLS 99.99%

    OF GERMS

    3.3 FL. OZ. (100ML) Label

  • INGREDIENTS AND APPEARANCE
    ANTIMICROBIAL 
    antimicrobial face and body spray liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72471-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    EUROPEAN ELDERBERRY (UNII: BQY1UBX046)  
    UNCARIA TOMENTOSA LEAF (UNII: 487U8M3D2P)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    WATER (UNII: 059QF0KO0R)  
    ECHINACEA PURPUREA (UNII: QI7G114Y98)  
    OREGANO (UNII: 0E5AT8T16U)  
    HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCYRRHIZA URALENSIS (UNII: 42B5YD8F0K)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    HYALURONIC ACID (UNII: S270N0TRQY)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72471-101-101 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/21/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E09/21/2020
    Labeler - VMP Cosmetics (022451337)
    Registrant - VMP Cosmetics (022451337)
    Establishment
    NameAddressID/FEIBusiness Operations
    VMP Cosmetics022451337manufacture(72471-101)
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!