CALIFORNIA ALOE FRESH SUN MILK description, usages, side effects, indications, overdosage, supplying and lots more!

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CALIFORNIA ALOE FRESH SUN MILK

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


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

Active Ingredients: Zinc Oxide 12.48%, Titanium Dioxide 2.00%

INACTIVE INGREDIENT

Ingredients:
CYCLOPENTASILOXANE, WATER, ISODODECANE, BUTYLENE GLYCOL, DICAPRYLYL ETHER, GLYCERIN, METHYL METHACRYLATE CROSSPOLYMER, ALCOHOL, BIOSACCHARIDE GUM-1, CAPRYLYL METHICONE, NIACINAMIDE, CAPRYLIC/CAPRIC/SUCCINIC TRIGLYCERIDE, PEG-10 DIMETHICONE, POLYMETHYLSILSESQUIOXANE, PORTULACA OLERACEA EXTRACT, DIMETHICONE, MAGNESIUM SULFATE, METHICONE, ALOE BARBADENSIS LEAF EXTRACT, SILICA, PHENOXYETHANOL, FRAGRANCE, POLYGLYCERYL-6 POLYRICINOLEATE, ALUMINUM HYDROXIDE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, CAPRYLYL GLYCOL, STEARIC ACID, GLYCERYL CAPRYLATE, MORINDA CITRIFOLIA EXTRACT, SEA WATER, TOCOPHERYL ACETATE, ADENOSINE, POLYURETHANE-11, HIBISCUS ROSA-SINENSIS FLOWER/LEAF EXTRACT

PURPOSE

Purpose: Brightening, Wrinkle-Improving, UV Protection

WARNINGS

Cautions:
For external use only.
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:
Take an adequate amount of the product and thoroughly apply on the areas exposed to the UV rays.

DOSAGE AND ADMINISTRATION

How to Use:
Take an adequate amount of the product and thoroughly apply on the areas exposed to the UV rays.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CALIFORNIA ALOE FRESH SUN MILK

CALIFORNIA ALOE FRESH SUN MILK

Zinc Oxide, Titanium Dioxide CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:51346-244
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Zinc Oxide Zinc oxide 6.24 mg
titanium dioxide 1 mg

Inactive Ingredients

Ingredient Name Strength
water
BUTYLENE GLYCOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:51346-244-01 50 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2014-02-01


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Be sure to consult your doctor before taking any medication!
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