Label: EQUATE FIRST AID ANTISEPTIC- povidone-iodine solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 10, 2023

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  • ACTIVE INGREDIENT

    Active Ingredient: Povidone-Iodine USP (10%)

    (1% available Iodine)

  • PURPOSE

    Purpose: First Aid Antiseptic

  • INDICATIONS & USAGE

    Use:

    First aid antiseptic to help prevent the risk of infection in minor cuts, scrapes and burns.

  • WARNINGS

    Warnings:

    For external use only

    Do not use

    • to the eyes or over large areas of the body
    • longer than a week unless directed by a doctor 
  • ASK DOCTOR

    Ask a doctor before use in case of deep or puncture wounds, animal bites, or serious burns

    Stop use and ask a doctor if condition persists or gets worse

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or consult a poison control center right away

  • Directions

    • clean the affacted area,
    • apply a small anount of the product to the area 1-3 times daily.
    • maybe covered with a sterile bandage.
    • if bandaged, let dry first.
  • OTHER SAFETY INFORMATION

    Other information

    • Store between 15-30C (59-86F)
  • INACTIVE INGREDIENT

    Inactive Ingredient

    Citric acid, disodium hydrogen phosphate, purified water

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    EQUATE FIRST AID ANTISEPTIC 
    povidone-iodine solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-230
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM PHOSPHATE DIBASIC DIHYDRATE (UNII: 94255I6E2T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-230-08237 mL in 1 BOTTLE; Type 0: Not a Combination Product10/10/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00310/10/2023
    Labeler - Walmart Inc. (051957769)
    Registrant - Lights Medical Manufacture Co., Ltd. (529128649)
    Establishment
    NameAddressID/FEIBusiness Operations
    Lights Medical Manufacture Co., Ltd.529128649manufacture(79903-230)
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