Medication Guide App

MYUNG HAN MI IN DO TWO WAY CAKE SPF35 PA NB23

Dosage form: powder
Ingredients: TITANIUM DIOXIDE 1.02g in 12g, ZINC OXIDE 0.35g in 12g
Labeler: THEFACESHOP CO., LTD.
NDC Code: 51523-018

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.

Drug Facts

Active Ingredients: TITANIUM DIOXIDE, ZINC OXIDE

Inactive Ingredients:

WATER, TALC, MICA(CI 77019), SILICA, NYLON-12, ETHYLHEXYL METHOXYCINNAMATE, BORON NITRIDE, METHYL METHACRYLATE CROSSPOLYMER, TRIMETHYLOLPROPANE TRIETHYLHEXANOATE, TRIETHYLHEXANOIN, IRON OXIDES(CI 77492), MAGNESIUM MYRISTATE, DIMETHICONE, METHICONE, MAGNESIUM STEARATE, CALCIUM CARBONATE, IRON OXIDES(CI 77491), HYDROGENATED LECITHIN, METHYLPARABEN, FRAGRANCE, IRON OXIDES(CI 77499), BUTYLPARABEN, SYNTHETIC BEESWAX, ULTRAMARINES(CI 77007), BISMUTH OXYCHLORIDE(CI 77163), NELUMBO NUCIFERA FLOWER EXTRACT, TRIETHOXYCAPRYLYLSILANE, CAPRYLIC/CAPRIC TRIGLYCERIDE, LYCIUM CHINENSE FRUIT EXTRACT, ANGELICA GIGAS ROOT EXTRACT, PORIA COCOS EXTRACT, CUSCUTA JAPONICA SEED EXTRACT, ACHYRANTHES BIDENTATA ROOT EXTRACT, PANAX GINSENG ROOT EXTRACT, POLYGONUM MULTIFLORUM ROOT EXTRACT, PHENOXYETHANOL, BUTYLENE GLYCOL, CHRYSANTHEMUM MORIFOLIUM FLOWER EXTRACT, JASMINUM OFFICINALE (JASMINE) OIL, ALTHAEA ROSEA FLOWER EXTRACT, ETHYLPARABEN, ISOBUTYLPARABEN, PROPYLPARABEN, LONICERA JAPONICA (HONEYSUCKLE) FLOWER EXTRACT, LOTUS CORNICULATUS FLOWER EXTRACT, DEXTRIN, MONASCUS EXTRACT, GARDENIA FLORIDA, FRUIT EXTRACT, SORGHUM VULGARE SEED/SKIN/STALK EXTRACT, CARTHAMUS TINCTORIUS (SAFFLOWER) FLOWER EXTRACT

Warnings:
When using this product
Keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if
Rash or irritation develops and lasts.

Directions:
Apply evenly before sun exposure and as needed.

MYUNG HAN MI IN DO TWO WAY CAKE  SPF35 PA NB23
titanium dioxide powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51523-018
Route of AdministrationCUTANEOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (TITANIUM) TITANIUM DIOXIDE1.02 g  in 12 g
ZINC OXIDE (ZINC CATION) ZINC OXIDE0.35 g  in 12 g
Packaging
#Item CodePackage Description
1NDC:51523-018-0112 g in 1 CARTON
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35204/01/2009
Labeler - THEFACESHOP CO., LTD. (688329416)

Revised: 07/2010
 
THEFACESHOP 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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