ANTISEPTIC SOLUTION solution

Antiseptic Solution by

Drug Labeling and Warnings

Antiseptic Solution by is a Prescription medication manufactured, distributed, or labeled by Grupo Salypro de Mexico, S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

ANTISEPTIC SOLUTION 
antiseptic solution solution

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 81760-310
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POTASSIUM PERMANGANATE (UNII: 00OT1QX5U4) (PERMANGANATE ION - UNII:2BL953CCZ2)	POTASSIUM PERMANGANATE	5.12 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81760-310-01	40 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	04/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/01/2021

Labeler - Grupo Salypro de Mexico, S.A. de C.V. (951596655)

Establishment
Name	Address	ID/FEI	Business Operations
Grupo Salypro de Mexico, S.A. de C.V.		951596655	manufacture(81760-310)