QIDILA WHITENING SKIN LIGHTENING CREAM (butylene glycol,butyrospermum parkii- shea butter,kyounin yu,tocopherol,ascorbic acid,niacinamide cream

QIDILA Whitening Skin Lightening Cream by

Drug Labeling and Warnings

QIDILA Whitening Skin Lightening Cream by is a Otc medication manufactured, distributed, or labeled by Beijing JUNGE Technology Co., Ltd., Zhejiang Ayan Biotech Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

BUTYLENE GLYCOL 5%
BUTYROSPERMUM PARKII (SHEA BUTTER) 3%
KYOUNIN YU 2%
TOCOPHEROL 1%
ASCORBIC ACID 0.05%
NIACINAMIDE 0.05%

Purpose

Whitening
Anti-wrinkle
Moisturizing
Nourishing
Anti-aging

Uses

1 .Clean and dry your skin.
2 . Apply a proper amount of the cream on desired area with your fingers, using a circular motion to massage the cream into the skin.
3 .Please apply it twice a day(morning and evening)

Warnings

For external use only. Keep out of reach of children.Avoid contact with eyes.

Keep out of reach of children

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

CAUTION

After using the product if irritation or rash appears,discontinue use.If irritation or
rash persists.consult your doctor.

DOSAGE

Approximately 0.1oz each time

Inactive Ingredients

AQUA,CAMELLIA JAPONICA SEED OIL,CETEARYL ALCOHOL,CETEARYL GLUCOSIDE,OLEA EUROPAEA (OLIVE) FRUIT OIL,CENTELLA ASIATICA ROOT EXTRACT,POLYGONUM CUSPIDATUM ROOT EXTRACT,SCUTELLARIA BAICALENSIS ROOT EXTRACT,CAMELLIA SINENSIS LEAF EXTRACT,GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT,CHAMOMILLA RECUTITA (MATRICARIA) FLOWER EXTRACT,ROSMARINUS OFFICINALIS (ROSEMARY) LEAF EXTRACT,PEARL POWDER,ARBUTIN,CARBOMER,ARGININE,SODIUM HYALURONATE,1,2-HEXANEDIOL,PROPYLENE GLYCOL,GLYCERYL CAPRYLATE,CAPRYLHYDROXAMIC ACID

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

QIDILA WHITENING SKIN LIGHTENING CREAM 
butylene glycol,butyrospermum parkii (shea butter),kyounin yu,tocopherol,ascorbic acid,niacinamide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85212-0006
Route of Administration	EXTRACORPOREAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOCOPHEROL (UNII: R0ZB2556P8) (TOCOPHEROL - UNII:R0ZB2556P8)	TOCOPHEROL	1 g  in 100 mL
BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y) (BUTYROSPERMUM PARKII (SHEA) BUTTER - UNII:K49155WL9Y)	BUTYROSPERMUM PARKII (SHEA) BUTTER	3 g  in 100 mL
PRUNUS ARMENIACA (APRICOT) KERNEL EXTRACT (UNII: 75356789IW) (PRUNUS ARMENIACA (APRICOT) KERNEL EXTRACT - UNII:75356789IW)	PRUNUS ARMENIACA (APRICOT) KERNEL EXTRACT	2 g  in 100 mL
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	0.05 g  in 100 mL
BUTYLENE GLYCOL (UNII: 3XUS85K0RA) (BUTYLENE GLYCOL - UNII:3XUS85K0RA)	BUTYLENE GLYCOL	5 g  in 100 mL
ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R)	ASCORBIC ACID	0.05 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CENTELLA ASIATICA ROOT (UNII: 8MXU1P42J0)	0.5 mL  in 100 mL
POLYGONUM CUSPIDATUM ROOT (UNII: 7TRV45YZF7)	0.5 mL  in 100 mL
OLEA EUROPAEA (OLIVE) FRUIT OIL (UNII: 6UYK2W1W1E)	1 mL  in 100 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	0.02 mL  in 100 mL
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)	0.005 mL  in 100 mL
CAMELLIA JAPONICA SEED OIL (UNII: U37N0S910T)	2 mL  in 100 mL
CARBOMER (UNII: 0A5MM307FC)	0.05 mL  in 100 mL
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)	0.0005 mL  in 100 mL
GLYCYRRHIZA GLABRA (LICORICE) ROOT (UNII: 2788Z9758H)	0.1 mL  in 100 mL
SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)	0.2 mL  in 100 mL
ARBUTIN (UNII: C5INA23HXF)	0.05 mL  in 100 mL
MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ)	0.1 mL  in 100 mL
AQUA (UNII: 059QF0KO0R)	80.4845 mL  in 100 mL
CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0)	0.2 mL  in 100 mL
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)	1.5 mL  in 100 mL
CETEARYL ALCOHOL (UNII: 2DMT128M1S)	2 mL  in 100 mL
1,2-HEXANEDIOL (UNII: TR046Y3K1G)	0.02 mL  in 100 mL
ROSEMARY (UNII: IJ67X351P9)	0.05 mL  in 100 mL
CALOPHYLLUM INOPHYLLUM SHELL POWDER (UNII: 32KAC96Q0G)	0.05 mL  in 100 mL
ARGININE (UNII: 94ZLA3W45F)	0.05 mL  in 100 mL
SODIUM HYALURONATE (UNII: YSE9PPT4TH)	0.02 mL  in 100 mL

Product Characteristics
Color		Score
Shape	FREEFORM	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85212-0006-1	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/01/2025

Labeler - Beijing JUNGE Technology Co., Ltd. (848718652)

Registrant - Beijing JUNGE Technology Co., Ltd. (848718652)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Ayan Biotech Co., Ltd.		544377996	manufacture(85212-0006)