NDC | 70341-620-01, 70341-620-02 |
Set ID | 81877218-4e5e-4143-aeea-8b241d848114 |
Category | HUMAN OTC DRUG LABEL |
Packager | The Saem International Co., Ltd. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Inactive ingredients:
Water, Cyclopentasiloxane, Dimethicone, Butylene Glycol, Cyclohexasiloxane, Butylene Glycol Dicaprylate/Dicaprate, Diethylhexyl Carbonate, Glycerin, Phenyl Trimethicone, PEG-10 Dimethicone, Alcohol Denat., Niacinamide, Sodium Chloride, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, Iron Oxides (CI 77492), Cetyl PEG/PPG-10/1 Dimethicone, Methyl Methacrylate Crosspolymer, PEG-10 Methyl Ether Dimethicone, Talc, Disteardimonium Hectorite, 1,2-Hexanediol, Iron Oxides (CI 77491), Caprylyl Glycol, Triethyl Citrate, Triethoxycaprylylsilane, Fragrance, Tocopheryl Acetate, Disodium EDTA, Betula Platyphylla Japonica Juice, Iron Oxides (CI 77499), Hydrogen Dimethicone, Ethylhexylglycerin, Adenosine, Propylene Glycol, Ethoxydiglycol, Rosa Centifolia Flower Water, Vaccinium Macrocarpon (Cranberry) Fruit Extract, Olea Europaea (Olive) Leaf Extract, Equisetum Arvense Extract, Adansonia Digitata Seed Extract, Sophora Japonica Flower Extract, Pentylene Glycol, Fructan, Nelumbo Nucifera Flower Water, Ceramide NP, Sodium Hyaluronate
- PURPOSE
-
WARNINGS
Warnings:
For external use only
1. In case of having following symptoms after using this, you're advised to stop using it immediately. If you keep using it, the symptoms will get worse and need to consult a dermatologist.
1) In case of having problems such as red rash, swollenness, itching, stimulation during usage.
2) In case of having the same symptoms above on the part you put this product on by direct sunlight.
2. You are banned to use it on the part where you have a scar, eczema, or dermatitis.
3. In case of getting it into your eyes, you have to wash it immediately.
4. Keep out of reach of babies and children.
- DESCRIPTION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SAEMMUL COVER FOUNDATION 01 LIGHT BEIGE
titanium dioxide, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70341-620 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Titanium Dioxide (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) Titanium Dioxide 2.00 g in 15 mL Zinc Oxide (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 0.21 g in 15 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70341-620-02 1 in 1 CARTON 05/01/2018 1 NDC:70341-620-01 15 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 05/01/2018 Labeler - The Saem International Co., Ltd. (689402402) Registrant - The Saem International Co., Ltd. (689402402) Establishment Name Address ID/FEI Business Operations Cosmecca Korea Co., Ltd. 688830827 manufacture(70341-620)