PLACENTA EX SUN BALM SPF50PLUS PA PLUS PLUS PLUS

Dosage form: cream
Ingredients: OCTINOXATE 0.84g in 12g, TITANIUM DIOXIDE 0.73g in 12g, ZINC OXIDE 0.59g in 12g
Labeler: NATURE REPUBLIC CO., LTD.
NDC Code: 51346-031

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: Ethylhexyl Methoxycinnamate 7%, Titanium Dioxide 6.1%, Zinc Oxide 4.9%

INACTIVE INGREDIENT

Inactive Ingredients:
Dicaprylyl Carbonate, Silica, Caprylic/Capric Triglyceride, Methicone, Aluminum Hydroxide, Stearic Acid, Mica, Triethoxycaprylylsilane, Ceresin, Dimethicone, Isoamyl p-Methoxycinnamate, Microcrystalline Wax, Polyethylene, Hydroxyapatite, Sorbitan Isostearate, Cetearyl Glucoside, Cetearyl Alcohol, Triethoxycaprylylsilane, Acetylated Sucrose Distearate, Cyclopentasiloxane, C30-45 Alkyl Cetearyl Dimethicone Crosspolymer, Methyl Methacrylate Crosspolymer, Ultramarines, Fragrance, Methylparaben, Butylene Glycol, Water, Glycine Soja (Soybean)Phytoplacenta Extract, Iron Oxides, Alcohol, Gentiana Lutea Root Extract, Achillea Millefolium Extract, Artemisia Absinthium Extract, Arnica Montana Flower Extract, Potassium Sorbate, Citrus Aurantium Dulcis (Orange) Fruit Water, 1,2-Hexanediol, Hydrolyzed Collagen

PURPOSE

Purpose: Sunscreen product with multi-functions of brightening and anti-aging care.

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: Apply an appropriate amount to the face using a gentle patting motion.

DOSAGE AND ADMINISTRATION

How to Use: Apply an appropriate amount to the face using a gentle patting motion.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

PLACENTA EX SUN BALM  SPF50PLUS PA PLUS PLUS PLUS
octinoxate, titanium dioxide, zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51346-031
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (OCTINOXATE) OCTINOXATE0.84 g  in 12 g
TITANIUM DIOXIDE (TITANIUM DIOXIDE) TITANIUM DIOXIDE0.73 g  in 12 g
ZINC OXIDE (ZINC OXIDE) ZINC OXIDE0.59 g  in 12 g
Inactive Ingredients
Ingredient NameStrength
DICAPRYLYL CARBONATE 
SILICON DIOXIDE 
MEDIUM-CHAIN TRIGLYCERIDES 
ALUMINUM HYDROXIDE 
STEARIC ACID 
Packaging
#Item CodePackage Description
1NDC:51346-031-0112 g in 1 CARTON
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35203/01/2012
Labeler - NATURE REPUBLIC CO., LTD. (631172020)
Registrant - NATURE REPUBLIC CO., LTD. (631172020)
Establishment
NameAddressID/FEIOperations
NATURE REPUBLIC CO., LTD.631172020manufacture(51346-031)

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.

Hide
(web3)