DR.DIFFERENT VITAACNAL TX NIGHT- capryloyl salicylic acid cream

Dr.Different VITAACNAL TX Night by

Drug Labeling and Warnings

Dr.Different VITAACNAL TX Night by is a Otc medication manufactured, distributed, or labeled by Dareun Cosmetics Co., Ltd., Ecoment. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Capryloyl Salicylic Acid 0.1%

INACTIVE INGREDIENTS

Water, Glycerin, Brassica Campestris (Rapeseed) Sterols, Cholesterol, Phytosteryl/Behenyl/Octyldodecyl Lauroyl Glutamate, 1,2-Hexanediol, Microcrystalline Cellulose, Polyglyceryl-10 Oleate, Hydrogenated Lecithin, Sodium Hyaluronate, Polyglutamic Acid, Ceramide NP, Tocopherol, Retinal, Stearic Acid, Oleic Acid, Disodium EDTA

PURPOSE

Acne treatment

WARNINGS

For external use only.
1. If there is any red spot, swallowing or itching by direct sunlight or if there is any other adverse effect during or after cosmetics use, consult with a doctor.
2. Refrain from using on the injured area.
3. Precaution for storage and handling.
a) Keep out of reach of children.
b) Keep away from direct sunlight.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Uses

■ Helps improve acne problem.

Directions

This product is for night use. At the final step of your nightly skincare routine or before going to bed, gently apply an adequate amount across your entire face.
*If you are trying this product for the first time, we recommend you to test a small amount before use.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR.DIFFERENT VITAACNAL TX NIGHT 
capryloyl salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81710-070
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Capryloyl Salicylic Acid (UNII: 5F7PJF6AA4) (Capryloyl Salicylic Acid - UNII:5F7PJF6AA4)	Capryloyl Salicylic Acid	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
RAPESEED STEROL (UNII: B46B6DD20U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81710-070-02	1 in 1 CARTON	04/01/2021
1	NDC: 81710-070-01	20 g in 1 TUBE; Type 0: Not a Combination Product

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

Labeler - Dareun Cosmetics Co., Ltd. (694894617)

Registrant - Dareun Cosmetics Co., Ltd. (694894617)

Establishment
Name	Address	ID/FEI	Business Operations
Ecoment		688485136	manufacture(81710-070)