Label: DR.DIFFERENT VITAACNAL TX NIGHT- capryloyl salicylic acid cream
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Contains inactivated NDC Code(s)
NDC Code(s): 81710-070-01, 81710-070-02 - Packager: Dareun Cosmetics Co., Ltd.
- Category: HUMAN OTC 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 April 12, 2021
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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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
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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
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR.DIFFERENT VITAACNAL TX NIGHT
capryloyl salicylic acid creamProduct 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)