Label: ANTISEPTIC SOLUTION solution

  • NDC Code(s): 81760-310-01
  • Packager: Grupo Salypro de Mexico, S.A. de C.V.
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated January 10, 2022

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

  • WARNING

    For external use on the skin only.
    Severe injury may result from use internally or as a douche. Avoid contact with mucous membranes."

  • INDICATIONS AND USAGE

    Astringent, Alkaline, for superficial and deep festering wounds. for 1st, 2nd and 3rd ulcers and burns. grade. Ideal for people with diabetes.Úpply directly without diluting, on the affected area or use an impregnated gauze.

  • DOSAGE AND ADMINISTRATION

    It Is Recommended to apply 3 to 5 times a day.

  • DOSAGE FORMS AND STRENGTHS

    Antiseptic Solution 40ml

  • CONTRAINDICATIONS

    Allergy or hypersensitivity to the active ingredient.

  • WARNINGS AND PRECAUTIONS

    There may be moderate burning or pain after the first applications of the solution, which usually disappear with the continuation of the treatment.

  • DRUG INTERACTIONS

    Free drug interactions. No patient presented adverse events related to treatment with Vikút®.

  • USE IN SPECIFIC POPULATIONS

    VIKÚT solution is indicated for pre and post-operative antisepsis and the delimitation of the surgical field. Antisepsis of minor and deep wounds, burns (1, 2, and 3rd degree), lacerations, pyoderma, acne and bacterial and fungal infections of the skin, scalp. In wounds where it is desired to accelerate the healing process such as traumatic surgical wounds, episiotomies, varicose ulcers, decubitus ulcers, where in addition to accelerating the healing process it is desired to eliminate or prevent the presence of pathogenic germs that could delay the process healing.

  • LABEL

    81760-310-01 40 mL Solution 40 mL Label

  • INGREDIENTS AND APPEARANCE
    ANTISEPTIC SOLUTION 
    antiseptic solution solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:81760-310
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POTASSIUM PERMANGANATE (UNII: 00OT1QX5U4) (PERMANGANATE ION - UNII:2BL953CCZ2) POTASSIUM PERMANGANATE5.12 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 28.06 g  in 100 g
    METHYL ALCOHOL (UNII: Y4S76JWI15) 60.75 g  in 100 g
    ACETYLSALICYLSALICYLIC ACID (UNII: VBE72MCP5L) 2.02 g  in 100 g
    .ALPHA.-(.ALPHA.-AMINOPROPYL)BENZYL ALCOHOL (UNII: S8TT5K3C8Y) 4.05 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81760-310-0140 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product04/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/01/2021
    Labeler - Grupo Salypro de Mexico, S.A. de C.V. (951596655)
    Establishment
    NameAddressID/FEIBusiness Operations
    Grupo Salypro de Mexico, S.A. de C.V.951596655manufacture(81760-310)