Label: MUKELIR ANTIBACTERIAL LIQUID FOR WASHING HANDS WITH ROCK SALT- disposable hand sanitizer spray

  • 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 May 12, 2020

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

View All Sections
  • Active Ingredient(s)

    0.10% Benzalkonium choride Purpose: Antiseptic

  • Purpose

    Antiseptic, Hand Sanitizer

  • Use

    The product is a topical product, which is suitable for cleaning and bacteriostasis of hand skin.

  • Warnings

    This product is only used for daily skin cleaning and cannot replace the medicine after infection physical therapy

  • Do not use

    If found turbid deterioraion

  • WHEN USING

    Children please use under the guidance of parants

  • STOP USE

    If found turbid deterioration do not use

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • Directions

    Spray directly on the skin. Spray your hands 3-5 times and rub until dry.

  • Other information

    Please keep it in a cool and dry place.

  • Inactive ingredients

    Sodium chloride, Purified water, C12-20 Alkyl glucoside, Propylene glycol, glycerin, essence

  • Package Label - Principal Display Panel

    60 mL NDC: 76620-001-01

    PDP

  • INGREDIENTS AND APPEARANCE
    MUKELIR ANTIBACTERIAL LIQUID FOR WASHING HANDS WITH ROCK SALT 
    disposable hand sanitizer spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76620-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76620-001-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product04/23/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/23/2020
    Labeler - Pingmei Shenma Group Henan Tianjian Daily Chemical Co., Ltd. (411229864)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pingmei Shenma Group Henan Tianjian Daily Chemical Co., Ltd.411229864manufacture(76620-001)
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!