Medication Guide App

BOTANICAL VANILLA SPF25 PA PLUS 02 VANILLA PINK

Dosage form: powder
Ingredients: TITANIUM DIOXIDE 1.525g in 25g, OCTINOXATE 0.5g in 25g, ZINC OXIDE 0.475g in 25g
Labeler: NATURE REPUBLIC CO., LTD.
NDC Code: 51346-011

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

ACTIVE INGREDIENT

Active Ingredients: TITANIUM DIOXIDE 6.1%, ETHYLHEXYL METHOXYCINNAMATE 2%, ZINC OXIDE 1.9%

INACTIVE INGREDIENT

Inactive Ingredients:
Talc, Methicone, Aluminum Starch Octenylsuccinate, Dimethicone, Methylparaben, Montmorillonite, Propylparaben, Fragrance, Iron Oxides, Mica, 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, Red 30

PURPOSE

Purpose: This vanilla-scented pact makes the skin moist 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

INDICATIONS AND USAGE

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

DOSAGE AND ADMINISTRATION

How to Use: At 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  SPF25 PA PLUS 02 VANILLA PINK
titanium dioxide, octinoxate, zinc oxide powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51346-011
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (TITANIUM DIOXIDE) TITANIUM DIOXIDE1.525 g  in 25 g
OCTINOXATE (OCTINOXATE) OCTINOXATE0.5 g  in 25 g
ZINC OXIDE (ZINC OXIDE) ZINC OXIDE0.475 g  in 25 g
Inactive Ingredients
Ingredient NameStrength
TALC 
ALUMINUM STARCH OCTENYLSUCCINATE 
DIMETHICONE 
METHYLPARABEN 
MONTMORILLONITE 
PROPYLPARABEN 
Packaging
#Item CodePackage Description
1NDC:51346-011-0125 g in 1 CARTON
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35202/01/2012
Labeler - NATURE REPUBLIC CO., LTD. (631172020)
Registrant - NATURE REPUBLIC CO., LTD. (631172020)
Establishment
NameAddressID/FEIOperations
NATURE REPUBLIC CO., LTD.631172020manufacture(51346-011)

Revised: 08/2012
 
NATURE REPUBLIC CO., LTD.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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