Label: DYNAMIC HAND SANITIZING WIPES- benzalkonium chloride cloth

  • NDC Code(s): 79203-001-01, 79203-001-02
  • Packager: Milky Way International Trading Corp
  • 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 February 8, 2022

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

View All Sections
  • Active Ingredient

    Purpose

    Antiseptic

  • USE

    ●For hand sanitizing to decrease bacteria on the skin.
    ●Apply topically to the skin to help prevent cross contamination.
    ● Recommended for repeated use.
    ●Dries in seconds.

  • Warning

    For external use only.
    Do not use in or contact the eyes.
    Stop use and ask a doctor if too much skin irritation or
    sensitivity develops or increases.

    keep out of reach of children. If swallowed, contact medical help or call Poison Control immediately.

  • Directions

    Open lid, gently pull back resealable label, pull out wipes to wipe
    hands throughly for 30 seconds.
    Reseal back after use to prevent moisture from evaporating.

  • Inactive ingredients

    Water, Phenoxyethanol, DMDM Hydantoin, Polysorbate 20,
    Ethylparaben, Methylparaben, Disodium EDTA, Sodium Citrate,
    Cetylpyridinium Chloride.

  • PRINCIPAL DISPLAY PANEL

    321

  • INGREDIENTS AND APPEARANCE
    DYNAMIC HAND SANITIZING WIPES 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79203-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.3 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DISODIUM EDTA-COPPER (UNII: 6V475AX06U)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
    ETHYLPARABEN (UNII: 14255EXE39)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79203-001-0150 in 1 BAG07/25/2020
    15.4 g in 1 PATCH; Type 0: Not a Combination Product
    2NDC:79203-001-0225 in 1 BAG07/25/2020
    25.4 g in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/25/2020
    Labeler - Milky Way International Trading Corp (083898916)
    Establishment
    NameAddressID/FEIBusiness Operations
    Kangna (Zhejiang) Medical Supplies Co., Ltd.554530173manufacture(79203-001)
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!