SHINE CONTROL MATTE EFFECT CREAM- glycerin, dimethicone cream

Shine Control Matte Effect Cream by

Drug Labeling and Warnings

Shine Control Matte Effect Cream by is a Otc medication manufactured, distributed, or labeled by CASMARA COSMETICS, SA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients Purpose

Active Ingredients Purpose

Glycerin 1.125%.................... Skin Protectant

Dimethicone 0.75%................Skin Protectant

Uses

. Anti aging cream with new regulative oil control ingredients

Uses

.Anti aging cream with new regulative oil control ingredients

Warnings

For external use only.

Do not use on damaged or broken skin.

When using this product keep our of the eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs.

Keep out of reach of children.

Whhen using this product do not get into eyes.

Children under 6 months: as a doctor.

Keep out of reach of children.

Warnings

Stop use and ask a doctor if rash occurs.

Questions or comments?

(305) 777-0548 M-F 9:00 am to 5:00 pm

Directions

. apply to clean face and neck until the product has been absorbed

. can be used in the morning and/or night.

Other information

. keep the product in a cool and dry place.

Inactive ingredients

Water, Avocado oil, Cetyl acetate, Cyclopentasiloxane, Egg yolk extract, Glyceryl stearate, Phenoxyethanol, Potassium azeloyl diglycinate, Acetylated lanolin alcohol, Sodium polyacrylate, Lecithin, Cetyl phosphate, Methylpropanediol, Perfluorodecalin, Oat Kernel extract, Jojoba seed oil, Trideceth-6, Fragrance, Ethylhexylglycerin, Tetrasodium glutamate diacetate, Ceramide NP
Sucrose palmitate, PEG/PPG-18/18 dimethicone, Rhamnose, Sodium benzoate, Potassium sorbate, Xanthan gum, Sodium hyaluronate, Silanetriol, Citric acid, Ascorbyl palmitate, BHT

Directions

. apply to clean face and neck until the product has been absorbed

. can be used in the morning and/or night.

Shine Control Matte Effect Cream

INGREDIENTS AND APPEARANCE

SHINE CONTROL MATTE EFFECT CREAM 
glycerin, dimethicone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 20151-096
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	1.12 mg  in 1 mL
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	DIMETHICONE	0.75 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BENZOATE (UNII: OJ245FE5EU)	0.01 mg  in 1 mL
ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P)	0.78 mg  in 1 mL
AVOCADO OIL (UNII: 6VNO72PFC1)	6 mg  in 1 mL
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)	0.016 mg  in 1 mL
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)	4.22 mg  in 1 mL
WATER (UNII: 059QF0KO0R)	71.25 mg  in 1 mL
CETYL ACETATE (UNII: 4Q43814HXS)	5.22 mg  in 1 mL
EGG YOLK (UNII: 4IPS17B70T)	2 mg  in 1 mL
METHYLPROPANEDIOL (UNII: N8F53B3R4R)	0.6 mg  in 1 mL
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)	2 mg  in 1 mL
XANTHAN GUM (UNII: TTV12P4NEE)	0.016 mg  in 1 mL
JOJOBA OIL (UNII: 724GKU717M)	0.22 mg  in 1 mL
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)	0.099 mg  in 1 mL
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)	0.1 mg  in 1 mL
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)	0.094 mg  in 1 mL
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)	0.75 mg  in 1 mL
PERFLUNAFENE (UNII: 54A06VV62N)	0.52 mg  in 1 mL
PHENOXYETHANOL (UNII: HIE492ZZ3T)	0.93 mg  in 1 mL
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)	0.62 mg  in 1 mL
HYDROLYZED JOJOBA ESTERS (POTASSIUM SALTS) (UNII: CH428W5O62)	0.42 mg  in 1 mL
CETYL PHOSPHATE (UNII: VT07D6X67O)	0.62 mg  in 1 mL
POTASSIUM AZELOYL DIGLYCINATE (UNII: N02RVN6NYP)	0.9 mg  in 1 mL
CERAMIDE NP (UNII: 4370DF050B)	0.09 mg  in 1 mL
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)	0.09 mg  in 1 mL
HYALURONATE SODIUM (UNII: YSE9PPT4TH)	0.01 mg  in 1 mL
SILANETRIOL (UNII: E52D0J3TS5)	0.009 mg  in 1 mL
ASCORBYL PALMITATE (UNII: QN83US2B0N)	0.0029 mg  in 1 mL
TRIDECETH-6 (UNII: 3T5PCR2H0C)	0.22 mg  in 1 mL
SUCROSE PALMITATE (UNII: 3OSQ643ZK5)	0.09 mg  in 1 mL
RHAMNOSE (UNII: QN34XC755A)	0.07 mg  in 1 mL
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)	0.017 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 20151-096-02	1 in 1 BOTTLE, PLASTIC	02/26/2017
1	NDC: 20151-096-01	50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	02/25/2017

Labeler - CASMARA COSMETICS, SA (464973544)

Registrant - CASMARA COSMETICS, SA (464973544)

Establishment
Name	Address	ID/FEI	Business Operations
CASMARA COSMETICS, SA		464973544	manufacture(20151-096)