Label: SANITIZING WIPES- 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 November 3, 2020

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  • Active Ingredient(s)

    Alcohol 75% v/v. Purpose: Antimicrobial

  • Purpose

    Antiseptic, Hand Sanitizer

  • Inactive ingredients

    WATER,PERFUME

  • Uses

    Suitable for skin cleaning and sterilization

  • Warnings

    For external use only.

    Flammable,keep away from fire or flame

  • Do not use

    • on open skin wounds
  • WHEN USING

    When using this product, avoid contact with eyes.In case of contact with eyes, rinse with water to remove.

  • STOP USE

    Stop use and ask a doctor if irritation or redness develop.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, seek medical attention immediately

  • Directions

    • Wet hands thoroughly with product and allow to dry without wiping
  • Other information

    • Do not store above 110F
    • May discolor some fabrics
  • Package Label - Principal Display Panel

    160PCS NDC 80991-001-01 FANJIA ALCOHOL

    160PCS NDC 80991-001-02 001-02

  • INGREDIENTS AND APPEARANCE
    SANITIZING WIPES 
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80991-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    FAGRAEA BERTEROANA FLOWER OIL (UNII: 6665W245VP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80991-001-01160 in 1 POUCH11/03/2020
    11.5 g in 1 APPLICATOR; Type 0: Not a Combination Product
    2NDC:80991-001-02160 in 1 CANISTER11/03/2020
    25 g in 1 APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A11/03/2020
    Labeler - Zhejiang Fanjia Medical Equipment Co., Ltd. (554552225)
    Registrant - Zhejiang Fanjia Medical Equipment Co., Ltd. (554552225)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Fanjia Medical Equipment Co., Ltd.554552225manufacture(80991-001) , label(80991-001)
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