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

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ALOE SUN ESSENCE

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

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredients: OCTINOXATE 7%, TITANIUM DIOXIDE 2.48%

Inactive ingredients:
WATER, ISOAMYL p-METHOXYCINNAMATE, BUTYLENE GLYCOL, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, CYCLOPENTASILOXANE, GLYCERIN, ISONONYL ISONONANOATE, MYRISTYL ALCOHOL, POLYSORBATE 80, CETYL ALCOHOL, STEARIC ACID, POLYGLYCERYL-3 METHYLGLUCOSE DISTEARATE, STEARETH-21, ALOE BARBADENSIS LEAF EXTRACT, BETA-GLUCAN, DIMETHICONE, PORTULACA OLERACEA EXTRACT, SORBITAN STEARATE, SODIUM POLYACRYLATE, POTASSIUM CETYL PHOSPHATE, ALUMINUM HYDROXIDE, 1,2-HEXANEDIOL, C13-14 ISOPARAFFIN, POLYACRYLAMIDE, LAURETH-7, CAMELLIA SINENSIS LEAF EXTRACT, ETHYLHEXYL STEARATE, BHT, TOCOPHERYL ACETATE, TRIDECETH-6, SODIUM HYALURONATE, DISODIUM EDTA, PHENOXYETHANOL, METHYLPARABEN, BUTYLPARABEN, 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 ESSENCE

ALOE SUN ESSENCE

OCTINOXATE CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:76214-030
Route of Administration CUTANEOUS DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 3.5 mL
titanium dioxide 1.24 mL

Inactive Ingredients

Ingredient Name Strength
water
BUTYLENE GLYCOL
CYCLOMETHICONE 5
GLYCERIN
ISONONYL ISONONANOATE
MYRISTYL ALCOHOL
polysorbate 80
CETYL ALCOHOL
STEARIC ACID
STEARETH-21
Aloe Vera Leaf
DIMETHICONE
PURSLANE
SORBITAN MONOSTEARATE
PHENOXYETHANOL
potassium cetyl phosphate
aluminum hydroxide
METHYLPARABEN
1,2-HEXANEDIOL
C13-14 ISOPARAFFIN
LAURETH-7
BUTYLPARABEN
GREEN TEA LEAF
ETHYLHEXYL STEARATE
BUTYLATED HYDROXYTOLUENE
TRIDECETH-6
HYALURONATE SODIUM
EDETATE DISODIUM

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:76214-030-01 50 in 1 CARTON

Marketing Information

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


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