Label: NTS ALCOHOL WIPES- ethanol 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 June 7, 2020

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Alcohol 75%

  • PURPOSE

    Purpose
    Antiseptic

  • INDICATIONS & USAGE

    Uses

    helps reduce bacteria on the skin that can potentially cause disease

  • WARNINGS

    Warnings
    For external use only.
    Flammable. Keep away from fire or flame.

    When using this product keep away from eyes. In case of eye contact, rinse eyes with water.

    Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

  • DOSAGE & ADMINISTRATION

    Directions

    • remove wipe from package and rub thoroughly over all surfaces of both hands
    • rub hands together until dry
    • supervise children under 6 years old
    • not recommended for infants
  • STORAGE AND HANDLING

    Other information

    • store between 15-30°C (59-86°F)
    • avoid freezing and excessive heat above 40°C (104°F)
  • INACTIVE INGREDIENT

    Inactive ingredient water

  • SPL UNCLASSIFIED SECTION

    Distributed by Nano Technology Solutions

    1212 Maple Drive, Suite B

    Troy, MI 48083

    (248) 234-4201

    Made in China

    nano-technologysolutions.com

  • PRINCIPAL DISPLAY PANEL

    Alcohol Wipes
    Alcohol 75%

    Antiseptic Wipes
    50 Wipes

    NTS Wipe PDP Final

    NTS Wipe Back Final

  • INGREDIENTS AND APPEARANCE
    NTS ALCOHOL WIPES 
    ethanol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76537-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76537-004-5050 in 1 PACKAGE06/08/2020
    14.7 mL in 1 APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E06/08/2020
    Labeler - Nano Technology Solutions (117496529)