- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive Ingredients: Water, Aloe Barbadensis Leaf Juice, Butylene Glycol, Glycerin, Sodium Hyaluronate, Betaine, PEG-11 Methyl Ether Dimethicone, Bis-PEG/PPG16/16-PEG/PPG-16/16-Dimethicone, Caprylic/Capric Triglyceride, Portulaca Oleracea Extract, Beta-Glucan, Calendula Officinalis Flower Extract, Camellia Sinensis Leaf Extract, Acetyl Hexapeptide-8, Caprylyl Glycol, Caprylhydroxamic Acid, Platinum, Copper Tripeptide-1, Arginine, Carbomer, Hydroxyethylcellulose, Disodium EDTA, Centella Asiatica Extract, Propolis Extract, Adenosine, Dipotassium Glycyrrhizate, Fragrance.
- PURPOSE
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WARNINGS
Warnings: 1. In case of having following symptoms after using this product, 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.
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS AND USAGE
- DOSAGE AND ADMINISTRATION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
VITAL FLUID I PLATINUM ANTI WRINKLE SERUM
allantoin creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60899-110 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Allantoin (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) Allantoin 0.15 mg in 30 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60899-110-01 30 mL in 1 CARTON; Type 0: Not a Combination Product 09/01/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 09/01/2013 Labeler - AMAROS CO., LTD. (690338801) Registrant - AMAROS CO., LTD. (690338801) Establishment Name Address ID/FEI Business Operations AMAROS CO., LTD. 690338801 manufacture(60899-110)