UV BOUNCE MIST description, usages, side effects, indications, overdosage, supplying and lots more!

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UV BOUNCE MIST

MIZON CO., LTD.
MIZON CO., LTD.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

Active Ingredients: Ethylhexyl Methoxycinnamate 7%, Ethylhexyl Salicylate 4%

INACTIVE INGREDIENT

Inactive Ingredients:
Water, Butylene Glycol, Caprylic/Capric Triglyceride, Phenylbenzimidazole Sulfonic Acid, Disiloxane, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Ceteareth-6 Olivate, Niacinamide, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Tromethamine, Dimethicone, Tocopheryl Acetate, Benzyl Alcohol, Microcrystalline Cellulose, Fragrance, Portulaca Oleracea Extract, Phenoxyethanol, Sodium Benzoate, Disodium EDTA, Potassium Sorbate, Glycerin, Cetearyl Olivate, Sorbitan Olivate, Adenosine, Cellulose Gum, Alpinia Officinarum Root Extract, Lactobacillus/Nelumbo Nucifera Seed Ferment Filtrate, Citrullus Lanatus (Watermelon) Fruit Extract, Terminalia Chebula Fruit Extract, Abies Koreana Leaf Extract, Aloe Barbadensis Leaf Juice

PURPOSE

Purpose: UVA/UVB Protection

WARNINGS

Warnings:
1. If following symptoms occur, stop use and consult a doctor: red spots, swelling, itcihng, irritation, or symtoms on applied skin under direct sunlight.
2. Do not use on scarred skin, or if you have dermatitis or eczema
3. Keep the cap close on its product
4. Keep away from direct sunlight or heat.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children:
Keep out of reach of babies and children

INDICATIONS AND USAGE

Indication and Usage:
Spray onto areas exposed to UV rays from about 20-30cm aways. (Use before or after makeup.)

DOSAGE AND ADMINISTRATION

Dosage and Administration:
2-3 time spry onto the areas that exposed to UV rays, and tap on applied skin for better aborption.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

UV BOUNCE MIST

UV BOUNCE MIST

OCTINOXATE, OCTISALATE SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57718-030
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 3.5 mg
OCTISALATE OCTISALATE 2 mg

Inactive Ingredients

Ingredient Name Strength
water
BUTYLENE GLYCOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57718-030-01 50 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2014-03-01


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Be sure to consult your doctor before taking any medication!
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