UV LOCK FLOWER MILD SUN description, usages, side effects, indications, overdosage, supplying and lots more!

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UV LOCK FLOWER MILD SUN

NATURE REPUBLIC CO., LTD.
NATURE REPUBLIC CO., LTD.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

Active Ingredients: Ethylhexyl Methoxycinnamate 7.5%, Titanium Dioxide 2.12%, Octocrylene 2%, Butyl Methoxydibenzoylmethane 1.2%

INACTIVE INGREDIENT

Inactive Ingredients:
Water, Cyclopentasiloxane, Dipropylene Glycol, Glycerin, Ethylhexyl Palmitate, Cyclohexasiloxane, Neopentyl Glycol Diheptanoate, Butylene Glycol, Pentylene Glycol, Triceteareth-4 Phosphate, Glycol Stearate, Dimethicone/Vinyl Dimethicone Crosspolymer, Glyceryl Stearate, Cetearyl Alcohol, Potassium Cetyl Phosphate, Polymethylsilsesquioxane, PEG-10 Dimethicone, PEG-2 Stearate, PEG-100 Stearate, Silica, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Phenoxyethanol, Fragrance(Parfum), Polyacrylate Crosspolymer-6, Water, Dimethicone, Disodium EDTA, Xanthan Gum, Glycine Soja (Soybean) Oil, Oenothera Biennis (Evening Primrose) Oil, Helianthus Annuus (Sunflower) Seed Oil, Rosa Damascena Flower Oil, Rosa Gallica Flower Extract, Caprylyl Glycol, 1,2-Hexanediol, Glycyrrhiza Glabra (Licorice) Root Extract, Rosa Canina Fruit Extract, Centella Asiatica Extract, Hordeum Vulgare Extract, Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract

PURPOSE

Purpose: UV Protection

WARNINGS

Cautions:
For external use only.
Avoid contact with eyes and mouth.
Discontinue use if signs of irritation or rashes appear.
Keep out of reach of children.
Replace the cap after use.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

INDICATIONS AND USAGE

How to Use: Evenly apply an appropriate amount to skin that can be easily exposed to UV rays.

DOSAGE AND ADMINISTRATION

How to Use: Evenly apply an appropriate amount to skin that can be easily exposed to UV rays.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

UV LOCK FLOWER MILD SUN

UV LOCK FLOWER MILD SUN

OCTINOXATE, Titanium Dioxide, Octocrylene, AVOBENZONE CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:51346-210
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 3.75 mg
titanium dioxide 1.06 mg
OCTOCRYLENE Octocrylene 1 mg
AVOBENZONE AVOBENZONE 0.6 mg

Inactive Ingredients

Ingredient Name Strength
water
DIPROPYLENE GLYCOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:51346-210-01 50 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2013-02-01


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