Label: LIGHTS POVINDONE IODINE SCRUB- povidone-iodine solution

  • NDC Code(s): 61333-205-01
  • Packager: Lights Medical Manufacture Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 28, 2023

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  • ACTIVE INGREDIENT

    Active Ingredient: Povidone-Iodine USP (7.5%)

  • PURPOSE

    Purpose: Antiseptic

  • INDICATIONS & USAGE

    Use:

    Antiseptic skin preparation

  • WARNINGS

    Warnings:

    Do not use if allergic to iodine

    For external use only

    Do not use in eyes

    Avoid pooling beneath patient. Prolonged exposure to wet solution may cause skiin irritation.

  • ASK DOCTOR

    Ask a doctor before use if injuries are

    deep or puncture wounds

    Serious burns

    Stop use and ask a doctor if 

    Redness, irritation, swelling or pain persisits or increases

    Infection occurs

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of a accidental ingestion,, seek professional assistance or consult a poison control center immediately

  • DOSAGE & ADMINISTRATION

    Directions:

    Apply locally as needed.

  • OTHER SAFETY INFORMATION

    Other information

    • Store at room temperature
    • 0.75% available iodine
    • Latax free
    • For hospital or professional use only
  • INACTIVE INGREDIENT

    Inactive Ingredient

    Citric acid, purified water, Disodium hydrogen phosphate

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    LIGHTS POVINDONE IODINE SCRUB 
    povidone-iodine solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61333-205
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE0.75 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM PHOSPHATE DIBASIC DIHYDRATE (UNII: 94255I6E2T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61333-205-01118 g in 1 BOTTLE; Type 0: Not a Combination Product07/18/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00307/18/2019
    Labeler - Lights Medical Manufacture Co., Ltd. (529128649)
    Registrant - Lights Medical Manufacture Co., Ltd. (529128649)
    Establishment
    NameAddressID/FEIBusiness Operations
    Lights Medical Manufacture Co., Ltd.529128649manufacture(61333-205)
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