OTC Medication Information: SIERO MO MORE ILLUMINATOR ROSY PINK

SIERO MO MORE ILLUMINATOR ROSY PINK- titanium dioxide stick
JNG KOREA CO.,LTD.

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 6.67%

INACTIVE INGREDIENT

Inactive ingredients: TRIETHYLHEXANOIN, ISOPROPYL ISOSTEARATE, POLYMETHYL METHACRYLATE, PROPYLENE GLYCOL DICAPRYLATE/DICAPRATE, HEXYL LAURATE, MICA, SYNTHETIC FLUORPHLOGOPITE, CERESIN, POLYETHYLENE, DIISOSTEARYL MALATE, HYDROGENATED POLYISOBUTENE, MICROCRYSTALLINE WAX, IRON OXIDES(CI 77491), DIPENTAERYTHRITYL HEXAHYDROXYSTEARATE/HEXASTEARATE/HEXAROSINATE, SORBITAN SESQUIOLEATE, POLYGLYCERYL-6 POLYRICINOLEATE, STEARALKONIUM HECTORITE, GLYCERYL CAPRYLATE, CAPRYLYL GLYCOL, FRAGRANCE, PROPYLENE CARBONATE, TOCOPHERYL ACETATE, TIN OXIDE, CARMINE, SAPPHIRE POWDER, AMETHYST POWDER, PEARL POWDER

PURPOSE

Purpose: Sunscreen

WARNINGS

Warnings: — Keep away from direct sunlight and high temperature. — For external use only Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear. Replace the cap after use. Keep Out of Reach of Children

DESCRIPTION

Uses: It is a stick type highlighter giving bright and radiant makeup.

Directions: Spread well on areas that need a highlighting effect.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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SIERO MO MORE ILLUMINATOR ROSY PINK
titanium dioxide stick
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:71472-200
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TITANIUM DIOXIDE (TITANIUM DIOXIDE) TITANIUM DIOXIDE 0.60 g in 9 g
Inactive Ingredients
Ingredient Name Strength
TRIETHYLHEXANOIN
ISOPROPYL ISOSTEARATE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:71472-200-02 1 CONTAINER in 1 CARTON contains a CONTAINER (71472-200-01)
1 NDC:71472-200-01 9 g in 1 CONTAINER This package is contained within the CARTON (71472-200-02)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part352 06/01/2017
Labeler — JNG KOREA CO.,LTD. (557796103)
Registrant — JNG KOREA CO.,LTD. (557796103)
Establishment
Name Address ID/FEI Operations
JNG KOREA CO.,LTD. 557796103 relabel (71472-200)
Establishment
Name Address ID/FEI Operations
Kolmar Korea Co., Ltd. 689847167 manufacture (71472-200)

Revised: 06/2017 JNG KOREA CO.,LTD.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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