Label: BEST-RX MOIST HAND WIPES- 70% ethyl alcohol cloth

  • 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 December 28, 2020

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

View All Sections
  • Active Ingredient(s)

    Alcohol 70% v/v;

  • Purpose

    Antibacterial

  • Use

    For hand sanitizing to decrease bacterial on the skin.

  • Warnings

    For external use only. Flammable. Keep away from heat or flame

  • Do not use

    • on infants less than 2 months of age
    • on open skin wounds
  • WHEN USING

    When using this product avoid contact with eyes, flush with water immediately if contact is made or irritation occurs.

  • STOP USE

    Discontinue use if irrtation or redness develops on skin.
    Contact a doctor if condition persists for more than 72 hours.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children: Unless under adult supervision.

  • Directions

    Tear open packet, wet hands thoroughly with towelette, allow hands to dry without wiping.
    Discard after single use.

  • Inactive ingredients

    Inactive ingredients: Water

  • Package Label - Principal Display Panel

    1 wipe in 1 pouch; NDC: 78183-001-01;

    1pcs

  • INGREDIENTS AND APPEARANCE
    BEST-RX MOIST HAND WIPES 
    70% ethyl alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79904-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 U  in 1 U
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79904-001-011 U in 1 BAG; Type 0: Not a Combination Product08/14/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/15/2020
    Labeler - BEST EQUIPMENT (039069751)
    Establishment
    NameAddressID/FEIBusiness Operations
    BEST EQUIPMENT039069751label(79904-001)
    Establishment
    NameAddressID/FEIBusiness Operations
    Kunming Ansheng Industry & Trade Co., Ltd.421081801manufacture(79904-001)
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!