CALIFORNIA ALOE DAILY MOISTURE SUN BLOCK description, usages, side effects, indications, overdosage, supplying and lots more!

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CALIFORNIA ALOE DAILY MOISTURE SUN BLOCK

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


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

Active Ingredients: Ethylhexyl Methoxycinnamate 7.50%, Titanium Dioxide 4.25%, Butyl Methoxydibenzoylmethane 2.50%, Ethylhexyl Salicylate 2.00%, Octocrylene 2.00%

INACTIVE INGREDIENT

Ingredients:
Water, Glycerin, Ethylhexyl Palmitate, Cyclopentasiloxane, 4-Methylbenzylidene Camphor, Cyclohexasiloxane, Butylene Glycol, Niacinamide, Neopentyl Glycol Diheptanoate, Silica, Cetearyl Alcohol, Glyceryl Stearate, PEG-100 Stearate, Triceteareth-4 Phosphate,
Glycol Stearate, Aloe Barbadensis Leaf Juice, Sorbitan Sesquioleate, Potassium Cetyl Phosphate, PEG-2 Stearate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tromethamine, Phenoxyethanol, Glyceryl Caprylate, Fragrance(Parfum), Caprylyl Glycol, Dimethicone,
Adenosine, Xanthan Gum, Disodium EDTA, Hibiscus Rosa-Sinensis Flower/Leaf Extract, Iron Oxides (CI 77491), Iron Oxides (CI 77492), Morinda Citrifolia Fruit Extract, Sea Water, Ethyl Hexanediol, Leuconostoc/Radish Root Ferment Filtrate, Sodium Benzoate,
Citric Acid, Pentylene Glycol, 1,2-Hexanediol

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

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

DOSAGE AND ADMINISTRATION

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 DAILY MOISTURE SUN BLOCK

CALIFORNIA ALOE DAILY MOISTURE SUN BLOCK

OCTINOXATE, Titanium Dioxide, AVOBENZONE, OCTISALATE, Octocrylene CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:51346-241
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 3.75 mg
titanium dioxide 2.21 mg
AVOBENZONE AVOBENZONE 1.25 mg
OCTISALATE OCTISALATE 1 mg
OCTOCRYLENE Octocrylene 1 mg

Inactive Ingredients

Ingredient Name Strength
water
GLYCERIN

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:51346-241-01 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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