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SKINMD LABORATORIES ReviTox blue

Dosage form
LIQUID
Labeler
Reviresco Co., Ltd.
Label updated
2018-11-28
Retrieved
2026-09-07
Active ingredients
Adenosine · Tranexamic acid
View original label and images on DailyMed ↗
ACTIVE INGREDIENT

Active ingredients: Adenosine 0.04%, Tranexamic acid 0.01%

INACTIVE INGREDIENT

Inactive ingredients:

Water, Panthenol, Elaeagnus Glabra Extract, Copper Tripeptide-1, Hydrolyzed Hyaluronic Acid, Acetyl Hexapeptide-8, Propanediol, Sodium Hyaluronate, Beta-Glucan, Rhodiola Sacra Root Extract, Butylene Glycol, Caprylyl/Capryl Glucoside, Hydroxyacetophenone, Sodium Cocoyl Glutamate, Glyceryl Caprylate, 1,2-Hexanediol, Sodium Surfactin, Citric Acid, Polyglyceryl-6 Oleate, Glycerin, Isopropyl Alcohol

PURPOSE

Purpose: Anti wrinkle

WARNINGS

Warnings:

1. Stop use if the following symptoms appear, continued use can worsen the situation. And please visit a doctor.
- Red spot, swelling, itching generate when using it.
- Above symptoms generates on applied area causing by UV.
2. Avoid applying to wound area, eczema, skin disease and so on.
3. Cautions for usage and storage
- Please cover the cap after use.
- Keep it out of reach of children.
- Keep it store in shadow and avoid heat and cold place to store.

KEEP OUT OF REACH OF CHILDREN

Keep it out of reach of children

Uses

Uses: For anti-wrinkle

Directions

Directions:

1. Clean your face carefully and remove the water remains.
2. Open the lid of the vial.
3. Put the transparent lid which can be found in the box on the solution bottle.
4. Take 2cc Revitoxblue solution on the back of your hand.
5. Smear Revitoxblue solution on the face where you want and pat the face to help absorb.
6. After using, please cover the transparent lid and store it in refrigerator.
7. Using it every morning and night.

Questions

Questions:
+82-2-1522-4259

PACKAGE LABEL

Caton Image 1

[Image in the official label — see DailyMed source]

PACKAGE LABEL

Carton Image 2

[Image in the official label — see DailyMed source]

DailyMed Set ID: ad87d4f8-e195-40a8-b17b-36e8e5817719 · Version 2
NDC: 71974-040