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

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THE FIRST 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, DICAPRYLYL CARBONATE, BIOSACCHARIDE GUM-1, BUTYLENE GLYCOL, PEG-10 DIMETHICONE, MAGNESIUM SULFATE, METHYL METHACRYLATE CROSSPOLYMER, PHENOXYETHANOL, METHICONE, ALUMINUM HYDROXIDE, ALUMINUM STEARATE, CAPRYLYL GLYCOL, GLYCERYL CAPRYLATE, CITRUS GRANDIS (GRAPEFRUIT) PEEL OIL, POLYGLYCERYL-6 POLYRICINOLEATE, SACCHAROMYCES FERMENT, OLEA EUROPAEA (OLIVE) FRUIT OIL, ACACIA SENEGAL FLOWER/STEM EXTRACT, CITRUS AURANTIFOLIA (LIME) OIL, RIBES NIGRUM (BLACK CURRANT) SEED OIL, ROSE FLOWER OIL, ILLICIUM VERUM (ANISE) FRUIT/SEED OIL, EUTERPE OLERACEA FRUIT EXTRACT, HYDROLYZED COLLAGEN, SODIUM LAUROYL SARCOSINATE, SOLUBLE COLLAGEN

Purpose

Purpose: This sun liquid, with its active ingredients of fermented enzyme, makes your skin look clear and transparent.

WARNINGS

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

Keep out of reach of children

Keep out of reach of children:

Keep out of reach of children

INDICATION AND USAGE

How to Use:
Gently shake the bottle before use.
Apply an appropriate amount to your face, following the skin's texture and softly pat your face
to enhance its absorption into your skin.

THE FIRST SUN DOSAGE AND ADMINISTRATION

How to Use:
Gently shake the bottle before use.
Apply an appropriate amount to your face, following the skin's texture and softly pat your face
to enhance its absorption into your skin.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

THE FIRST SUN

THE FIRST SUN

OCTINOXATE, ZINC OXIDE, OCTISALATE, TITANIUM DIOXIDE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:51346-001
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 3 g
Zinc Oxide Zinc oxide 2.61 g
OCTISALATE OCTISALATE 2 g
titanium dioxide 1 g

Inactive Ingredients

Ingredient Name Strength
water
CYCLOMETHICONE 5
ALCOHOL
DICAPRYLYL CARBONATE
BUTYLENE GLYCOL
PHENOXYETHANOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:51346-001-01 40 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-03-01


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