UROSE FULL COVERAGE CREAM- full coverage cream cream

UROSE Full Coverage Cream by

Drug Labeling and Warnings

UROSE Full Coverage Cream by is a Otc medication manufactured, distributed, or labeled by Guangzhou Meixi Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

TITANIUM DIOXIDE：6.65%
ETHYLHEXYL METHOXYCINNAMATE： 7%
ETHYLHEXYL SALICYLATE： 2%

Purpose

Moisturizing, anti-aging, sun protection, and concealing

Use

Product features: touch the skin as smooth as cream mousse, and facial integration to make the entire makeup naturally flawless, more texture, just the right amount of gloss, as if born with flawless skin, to create the exclusive elegant fog makeup feeling.

Warnings

For external use only

Do not use

Do not use on damaged or broken skin.

When Using

When using this product
keep out of eyes. Rinse with wate to remove
Stop use and ask doctor if rash occurs.

Stop Use

Stop use and ask doctor if rash occurs

Ask Doctor

Children under 6 months of age

Keep Oot Of Reach Of Children

Keep out of reach of children. lfswallowed, get medical help orcontact Poison Control Center right away

Directions

After basic skin care, apply liberally and evenly 15 minutes prior to sun exposure. Or gently dot on the forehead, cheeks, chin and nose wings, and then spread evenly on the skin surface

Other information

Storage conditions: Protected from light, ventilated, dry place.

Inactive ingredients

WATER,GLYCERIN,CYCLOPENTASILOXANE,DIMETHICONE,PROPYLENE GLYCOL,CETYL PEG/PPG-10/1 DIMETHICONE,POLYMETHYLSILSESQUIOXANE,CI 77492,CYCLOHEXASILOXANE,MAGNESIUM SULFATE,LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE,SILICA,SORBITAN SESQUIOLEATE,CI 77491,1,2-HEXANEDIOL,DISTEARDIMONIUM HECTORITE,PHENOXYETHANOL,TRIETHOXYCAPRYLYLSILANE,CI 77499,ALUMINUM HYDROXIDE,CITRUS AURANTIUM BERGAMIA (BERGAMOT) FRUIT OIL,CITRUS AURANTIUM DULCIS (ORANGE) PEEL OIL,ETHYLHEXYLGLYCERIN,PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE,TOCOPHEROL,BUTYLENE GLYCOL,GENTIANA SCABRA ROOT EXTRACT,CORDYCEPS SINENSIS EXTRACT,XANTHAN GUM,HYDROXYACETOPHENONE,CAPRYLYL GLYCOL,GLUCOSE,SODIUM HYALURONATE,CHONDRUS CRISPUS EXTRACT,HYDROXYPROPYLTRIMONIUM HYALURONATE,HYDROLYZED HYALURONIC ACID,SODIUM ACETYLATED HYALURONATE,HYALURONIC ACID,HYDROLYZED SODIUM HYALURONATE,POTASSIUM HYALURONATE,SODIUM HYALURONATE CROSSPOLYMER

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

UROSE FULL COVERAGE CREAM 
full coverage cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84167-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	2 g  in 100 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7 g  in 100 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	6.65 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)
XANTHAN GUM (UNII: TTV12P4NEE)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
MAGNESIUM SULFATE (UNII: DE08037SAB)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
POLYGLUTAMIC ACID (33000 MW) (UNII: JGC3VZ3H7Z)
OPHIOCORDYCEPS SINENSIS (UNII: 8Q1GYP08KU)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
BERGAMOT OIL (UNII: 39W1PKE3JI)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)
HYALURONIC ACID (UNII: S270N0TRQY)
POTASSIUM (UNII: RWP5GA015D)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
TOCOPHEROL (UNII: R0ZB2556P8)
FERRIC OXIDE RED (UNII: 1K09F3G675)
SODIUM POLYGLUTAMATE (33000 MW) (UNII: GPR9D9A7FN)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
DIMETHICONE (UNII: 92RU3N3Y1O)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 4) (UNII: 8INO2K35FA)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
GENTIANA SCABRA ROOT (UNII: GXZ33VNT92)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
ORANGE OIL (UNII: AKN3KSD11B)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84167-003-01	35 g in 1 TUBE; Type 0: Not a Combination Product	09/12/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	09/12/2024

Labeler - Guangzhou Meixi Biotechnology Co., Ltd. (625724571)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Meixi Biotechnology Co., Ltd.		625724571	manufacture(84167-003)