LANIMPRESS DARK ANTI-AGING CREAM liquid

LANIMPRESS Dark Anti-aging cream by

Drug Labeling and Warnings

LANIMPRESS Dark Anti-aging cream by is a Otc medication manufactured, distributed, or labeled by Shenzhen Zhumeng Times Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

RETINOL 1%...... Wrinkle treatment

Purpose

To help smooth the look of wrinkles, even skin tone

Uses

Smooth evenly over your cleansed face and neck morning and night.

Contraindications, Precautions, Warnings, and Instructions

For external use only

Do not use on damaged or broken skin

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

Stop use and ask a doctor if rash occurs

Keep out of reach of children.lf swallowed, get medical help or contact a Poison Control Center right away.

Dosage and administration

For external use only.

Do not use

Stop use and ask a doctor if rash occurs

When using section

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

stop use

Do not use on open wounds or allergic skin.

Keep out of reach of children.

If sxralowed, get medical help or contact a Poison Conirol Cenler ngiht away.

Inactive ingredients

AQUA,PROPYLENE GLYCOL,CETEARYL ALCOHOL,ETHYLHEXYL PALMITATE,MALUS DOMESTICA FRUIT EXTRACT,ELASTIN,HYDROXYPROLINE,CETEARYL ALCOHOL,CETEARYL GLUCOSIDE,ERYTHRITOL,GLYCERYL STEARATE,PEG-100 STEARATE,CYCLOPENTASILOXANE,CYCLOHEXASILOXANE,DIMETHICONE,HYDROLYZED COLLAGEN,PENTYLENE GLYCOL,CAPRYLHYDROXAMIC ACID,GLYCERYL CAPRYLATE,CARBOMER,METHYLPARABEN,TRIETHANOLAMINE,SODIUM HYALURONATE,TOCOPHEROL,NIACINAMIDE,DISODIUM EDTA

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LANIMPRESS DARK ANTI-AGING CREAM 
lanimpress dark anti-aging cream liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84372-027
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RETINOL (UNII: G2SH0XKK91) (RETINOL - UNII:G2SH0XKK91)	RETINOL	1 g  in 50 g

Inactive Ingredients
Ingredient Name	Strength
METHYLPARABEN (UNII: A2I8C7HI9T)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
TOCOPHEROL (UNII: R0ZB2556P8)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
TROLAMINE (UNII: 9O3K93S3TK)
PEG-100 STEARATE (UNII: YD01N1999R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
GLYCERYL DISTEARATE (UNII: 73071MW2KM)
ERYTHRITOL (UNII: RA96B954X6)
APPLE (UNII: B423VGH5S9)
ELASTIN (HUMAN) (UNII: VRC4754D50)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
HYDROXYPROLINE (UNII: RMB44WO89X)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84372-027-01	50 g in 1 PACKET; Type 0: Not a Combination Product	08/19/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	08/19/2024

Labeler - Shenzhen Zhumeng Times Technology Co., Ltd. (631852731)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Zhumeng Times Technology Co., Ltd.		631852731	manufacture(84372-027)