IBEALEE DARK SPOT CORRECTOR CREAM cream

iBeaLee Dark Spot Corrector Cream by

Drug Labeling and Warnings

iBeaLee Dark Spot Corrector Cream by is a Otc medication manufactured, distributed, or labeled by Shenzhen Yikai Electronic Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Niacinamide 5%

Purpose

Dark Spot Corrector

Warnings

WARNINGS:Keep out of reach of children. For external use only. Before using, test for sensitivity on a small area of skin.

Do not use

Do not use on damaged skin. Use only as directed. Avoid contact with eyes. Rinse with warm water to remove. Stop use and consult your physician if rash occurs. Do not ingest. If swallowed, get medical help or contact a Poison Control Center right away! Do not use if safety sealis broken or missing. Store in a cool, dry place.

Keep Oot Of Reach Of Children

Keep out of reach of children

Directions

Cleanse the application area and pat dry. Gently massage a thin layer into the affected area of skin until fully absorbed. Protect treated skin from sunlight by following up with an SPF 30+ sunscreen.

Inactive ingredients

Water, Sunflower Oil, Caprylyl Caprylate/Caprate,Glycerin,Trideceth-6, Aloe Vera, Niacinamide, Glycyrrhiza Glabra Extract, Morus Alba Root Extract, Hydrolyzed Oat Protein,Ethyl Ascorbic Acid, Alpha Arbutin, Hyaluronic Acid, Phenoxyethanol,Green Tea Extract, Tetrapeptide-21, Potassium Sorbate, Citric Acid,Xanthan Gum, Tocopherol, Soy Isoflavones, Cistus Ladaniferus Oil,Lemon Essential Oil.

Use

Remove dark spots on face.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

IBEALEE DARK SPOT CORRECTOR CREAM 
ibealee dark spot corrector cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83809-016
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SUNFLOWER OIL (UNII: 3W1JG795YI)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
XANTHAN GUM (UNII: TTV12P4NEE)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P)
ALPHA-ARBUTIN (UNII: 72VUP07IT5)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
TOCOPHEROL (UNII: R0ZB2556P8)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
MORUS ALBA ROOT (UNII: CST1G9BZGD)
CAPRYLYL CAPRYLATE/CAPRATE (UNII: 22MCG4RSMR)
GELATIN HYDROLYSATE (PORCINE SKIN, MW 3000) (UNII: 0K9R94573C)
HYALURONIC ACID (UNII: S270N0TRQY)
TETRAPEPTIDE-21 (UNII: 179JUC43HU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83809-016-01	20 g in 1 CANISTER; Type 0: Not a Combination Product	12/26/2023
2	NDC: 83809-016-02	50 g in 1 CANISTER; Type 0: Not a Combination Product	12/26/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	12/26/2023

Labeler - Shenzhen Yikai Electronic Technology Co., Ltd. (700426808)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Yikai Electronic Technology Co., Ltd.		700426808	label(83809-016) , manufacture(83809-016)