BOTANICAL VANILLA description, usages, side effects, indications, overdosage, supplying and lots more!

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BOTANICAL VANILLA

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


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

Active Ingredients: Titanium Dioxide 6.2%, Ethylhexyl Methoxycinnamate 2%, Zinc Oxide 1.9%

INACTIVE INGREDIENT

Inactive Ingredients:
Talc, Methicone, Aluminum Starch Octenylsuccinate, Dimethicone, Iron Oxides, Mica, Methylparaben, Montmorillonite, Propylparaben, Fragrance, Olea Europaea (Olive) Fruit Oil, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Cedrus Atlantica Bark Oil, Citrus Aurantium Dulcis (Orange) Fruit Extract, Citrus Grandis (Grapefruit) Fruit Extract, Lavandula Angustifolia (Lavender) Flower/Leaf/Stem Extract, Citrus Aurantifolia (Lime) Oil, Coriandrum Sativum (Coriander) Fruit Oil, Salvia Officinalis (Sage) Oil, Artemisia Absinthium Extract, Chamomilla Recutita (Matricaria) Flower Extract, Vanilla Planifolia Fruit Extract, Santalum Album (Sandalwood) Oil

PURPOSE

Purpose: This vanilla-scented powder makes the skin smooth with a matte finish.

WARNINGS

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

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

BOTANICAL VANILLA INDICATIONS AND USAGE

How to Use: As the last step of make up or touch up, apply an appropriate amount to the face using a puff and gently pat the skin.

BOTANICAL VANILLA DOSAGE AND ADMINISTRATION

How to Use: As the last step of make up or touch up, apply an appropriate amount to the face using a puff and gently pat the skin.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

BOTANICAL VANILLA

BOTANICAL VANILLA

TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:51346-010
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
titanium dioxide 1.55 g
OCTINOXATE OCTINOXATE 0.5 g
Zinc Oxide Zinc oxide 0.475 g

Inactive Ingredients

Ingredient Name Strength
talc
ALUMINUM STARCH OCTENYLSUCCINATE
DIMETHICONE
METHYLPARABEN
MONTMORILLONITE
PROPYLPARABEN

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:51346-010-01 25 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-02-01


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Be sure to consult your doctor before taking any medication!
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