DR.DIFFERENT VITAACNAL TX NIGHT- capryloyl salicylic acid cream 
Dareun Cosmetics Co., Ltd.

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.

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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

Image of carton

DR.DIFFERENT VITAACNAL TX NIGHT 
capryloyl salicylic acid cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81710-070
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Capryloyl Salicylic Acid (UNII: 5F7PJF6AA4) (Capryloyl Salicylic Acid - UNII:5F7PJF6AA4) Capryloyl Salicylic Acid0.1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Glycerin (UNII: PDC6A3C0OX)  
RAPESEED STEROL (UNII: B46B6DD20U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81710-070-021 in 1 CARTON04/01/2021
1NDC:81710-070-0120 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/01/2021
Labeler - Dareun Cosmetics Co., Ltd. (694894617)
Registrant - Dareun Cosmetics Co., Ltd. (694894617)
Establishment
NameAddressID/FEIBusiness Operations
Ecoment688485136manufacture(81710-070)

Revised: 4/2021
Document Id: 5a22b6be-fc4c-49be-aac9-1fd6e3d40e38
Set id: 1a170ed6-b3f0-4b51-a57f-a05d5ae24dc9
Version: 1
Effective Time: 20210412
 
Dareun Cosmetics Co., Ltd.