SKIN 79 THE PRESTIGE BEBLESH BALM (5G)- zinc oxide, titanium dioxide cream

SKIN 79 The Prestige Beblesh Balm (5g) by

Drug Labeling and Warnings

SKIN 79 The Prestige Beblesh Balm (5g) by is a Otc medication manufactured, distributed, or labeled by WIZCOZ CORPORATION LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PRINCIPAL DISPLAY PANEL

ACTIVE INGREDIENT

INGREDIENTS:

WATER, TITANIUM DIOXIDE, CYCLOPENTASILOXANE, PHENYL TRIMETHICONE, BUTYLENE GLYCOL, BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE, ZINC OXIDE, DIMETHICONE, C12-15 ALKYL BENZOATE, CETYL PEG/PPG-10/1 DIMETHICONE, HYDROGENATED POLYDECENE, ARBUTIN, HEXYL LAURATE, POLYGLYCERYL-4 ISOSTEARATE, SORBITAN ISOSTEARATE, NATTO GUM, GLYCERIN, MICA, CYCLOHEXASILOXANE, TALC, SORBITAN OLIVATE, OZOKERITE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, SODIUM CHLORIDE, DISTEARDIMONIUM HECTORITE, ALUMINUM HYDROXIDE, STEARIC ACID, TRIEHOXYCAPRYLSILANE, DIMETHICONE/METHICONE COPOLYMER, CALCIUM STEARATE, PROPYLENE CARBONATE, TOCOPHEROL ACETATE, HUMAN OLIGOPEPTIDE-1, ALOE BARBADENSIS LEAF JUICE, HYDROLIZED COLLAGE, NELUMBIUM SPECIOSUM FLOWER EXTRACT, CAVIAR EXTRACT, UBIQUINONE, PORTULACA OLERACEA EXTRACT, CAMELLIA SINENSIS LEAF EXTRACT, ACETYL HEXAPEPTIDE-8, ADENOSINE, DISODIUM EDTA, ASPARAGUS LUCIDUS ROOT EXTRACT, TUSSILAGO FARFARA (COLTSFOOT) FLOWER EXTRACT, LAMINARIA JAPONICA EXTRACT, DIAMOND POWDER, AMETHYST POWDER, PEARL POWDER, CORAL POWDER, TOURMALIN, CERAMIDE 3, GOLD, HESPERIDIN METHYL CHALCONE, STEARETH-20, DIPEPTIDE-2, PALMITOYL TETRAPEPTIDE-7, COPPER TRIPEPTIDE-1, LECITHIN, DEA-CETYL PHOSPHATE, RETINYL PALMITATE, SUCROSE DISTEARATE, SODIUM ASCORBYL PHOSPHATE, PANTHENOL, SILK AMINO ACIDES, ASCORBIN ACID, METHYLPARABEN, BUTYLPARABEN, PROPYLPARABEN, FRAGRANCE, IRON OXIDE RED, IRON OXIDE YELLOW, IRON OXIDE BLACK

WHEN USING

DIRECTIONS:

Use it proper quantity on the area of your face like patting at the last step of skin care.

INGREDIENTS AND APPEARANCE

SKIN 79 THE PRESTIGE BEBLESH BALM (5G) 
zinc oxide, titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49715-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC - UNII:J41CSQ7QDS)	ZINC OXIDE	0.19 g  in 5 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM - UNII:D1JT611TNE)	TITANIUM DIOXIDE	0.312 g  in 5 g

Inactive Ingredients
Ingredient Name	Strength
DIMETHICONE (UNII: 92RU3N3Y1O)	0.175 g  in 5 g
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)	0.025 g  in 5 g

Product Characteristics
Color	brown (Brown)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49715-004-01	5 g in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	12/01/2009

Labeler - WIZCOZ CORPORATION LTD (690397273)

Registrant - WIZCOZ CORPORATION LTD (690397273)

Establishment
Name	Address	ID/FEI	Business Operations
WIZCOZ CORPORATION LTD		690397273	manufacture