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

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ALOE SUN

SKINFOOD CO., LTD.
SKINFOOD CO., LTD.

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredients: OCTINOXATE 7%, ENSULIZOLE 2%

Inactive ingredients:
WATER, C12-15 ALKYL BENZOATE, 4-METHYLBENZYLIDENE CAMPHOR, BUTYLENE GLYCOL, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, CAPRYLIC/CAPRIC TRIGLYCERIDE, CETEARETH-6 OLIVATE, PEG-7 GLYCERYL COCOATE, ALOE BARBADENSIS LEAF EXTRACT, C12-20 ALKYL GLUCOSIDE, C14-22 ALCOHOLS, DIMETHICONE, MALPIGHIA GLABRA(ACEROLA) FRUIT EXTRACT, GLYCERIN, SODIUM HYDROXIDE, CELLULOSE GUM, CETEARYL OLIVATE, SORBITAN OLIVATE, MICROCRYSTALLINE CELLULOSE, DISODIUM EDTA, ETHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, METHYLPARABEN, PROPYLPARABEN, FRAGRANCE

Purpose

Purpose: Protects skin from UV rays.

Warnings:
For external use only. Avoid contact with eyes.
Discontinue use if signs of irritation appear.

Keep out of reach of children:
Keep out of reach of children.

Uses

Indication and usage:
Use at the end of your daily skincare regimen. Apply liberally onto face and body before sun exposure avoiding the eye area.

Dosage and administration:
For best results, apply at least 15 to 20 minutes before sun exposure.
Reapply frequently while out in the sun.

ALOE SUN

ALOE SUN

OCTINOXATE SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:76214-019
Route of Administration CUTANEOUS DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 7 mL
Ensulizole Ensulizole 2 mL

Inactive Ingredients

Ingredient Name Strength
water
ENZACAMENE
ALKYL (C12-15) BENZOATE
BUTYLENE GLYCOL
BEMOTRIZINOL
MEDIUM-CHAIN TRIGLYCERIDES
Aloe Vera Leaf
C12-20 ALKYL GLUCOSIDE
c14-22 alcohols
DIMETHICONE
GLYCERIN
METHYLPARABEN
SODIUM HYDROXIDE
CARBOXYMETHYLCELLULOSE SODIUM
CETEARYL OLIVATE
SORBITAN OLIVATE
PROPYLPARABEN
EDETATE DISODIUM
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:76214-019-01 100 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-03-01


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