UV LOCK ULTRA MILK SUN description, usages, side effects, indications, overdosage, supplying and lots more!

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UV LOCK ULTRA MILK SUN

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


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

Active Ingredients: ETHYLHEXYL METHOXYCINNAMATE 7.5%, ZINC OXIDE 6.5%, ETHYLHEXYL SALICYLATE 5%, TITANIUM DIOXIDE 2.5%

INACTIVE INGREDIENT

Inactive Ingredients:
WATER, CYCLOPENTASILOXANE, ALCOHOL,BUTYLENE GLYCOL, DIPROPYLENE GLYCOL, ISODECYL NEOPENTANOATE, METHYL METHACRYLATE CROSSPOLYMER, PEG-10 DIMETHICONE, MAGNESIUM SULFATE, PHENOXYETHANOL, CALCIUM ALUMINUM BOROSILICATE, FRAGRANCE, METHICONE, ALUMINUM HYDROXIDE, ALUMINUM STEARATE, SILICA, CAPRYLYL GLYCOL, GLYCERYL CAPRYLATE, POLYGLYCERYL-6 POLYRICINOLEATE, OPUNTIA FICUS-INDICA EXTRACT, PORTULACA OLERACEA EXTRACT, ARNICA MONTANA FLOWER EXTRACT, CENTAUREA CYANUS FLOWER EXTRACT, DIANTHUS CARYOPHYLLUS FLOWER EXTRACT, FREESIA REFRACTA EXTRACT, IRIS VERSICOLOR EXTRACT, JASMINUM OFFICINALE (JASMINE) FLOWER/LEAF EXTRACT, ZANTEDESCHIA AETHIOPICA FLOWER/STEM EXTRACT, CELLULOSE GUM, MICROCRYSTALLINE CELLULOSE

PURPOSE

Purpose: Strong milk sun block with daily skincare effects.

WARNINGS


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

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

UV LOCK ULTRA MILK SUN INDICATIONS AND USAGE

How to Use: Shake 3-5 times before use. Evenly apply an appropriate amount to skin that is exposed to UV rays.

UV LOCK ULTRA MILK SUN DOSAGE AND ADMINISTRATION

How to Use: Shake 3-5 times before use. Evenly apply an appropriate amount to skin that is exposed to UV rays.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

UV LOCK ULTRA MILK SUN

UV LOCK ULTRA MILK SUN

OCTINOXATE, ZINC OXIDE, OCTISALATE, TITANIUM DIOXIDE CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:51346-042
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 3.75 g
Zinc Oxide Zinc oxide 3.25 g
OCTISALATE OCTISALATE 2.50 g
titanium dioxide 1.25 g

Inactive Ingredients

Ingredient Name Strength
water
CYCLOMETHICONE 5
ALCOHOL
BUTYLENE GLYCOL
DIPROPYLENE GLYCOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:51346-042-01 50 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-01-02


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