DR.JUCRE REBIRTH WHITE BOOSTER- niacinamide liquid 
NATURECELL CO., LTD.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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ACTIVE INGREDIENTS

Niacinamide 2.0%

INACTIVE INGREDIENTS

Water, PEG/PPG-17/6 Copolymer, Glycerin, Human Adipose Derived Stem Cell Conditioned Media, Butylene Glycol, Diglycerin, Pentylene Glycol, Betaine, Dipropylene Glycol, Bis-PEG-18 Methyl Ether Dimethyl Silane, Phenoxyethanol, C12-14 Alketh-12, Dimethicone, Carbomer, Tromethamine, Cellulose Gum, Lecithin, Mica (CI 77019), Fragrance(Parfum), Biosaccharide Gum-1, Titanium Dioxide (CI 77891), Sodium Hyaluronate, Sodium Phytate, Iron Oxides (CI 77491), Gold (CI 77480), BHT, Plankton Extract

PURPOSE

Skin Brightening

WARNINGS

For external use only.
Avoid contact with eyes.
Discontinue use if signs of irritation or rashes appear.
Replace the cap after use.
Refrain from using it on wounded areas.
Keep out of reach of children.

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children.

Uses

■ Helps brighten skin tone

Directions

■ Apply an appropriate amount evenly on the skin.

Other Information

■ Do not store this product in an inappropriate place such as high or low temperatures or under direct sun light.

Questions

■ www.ibiostar.com
■ Tel (424)227-9568

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

DR.JUCRE REBIRTH WHITE BOOSTER 
niacinamide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83071-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide2.0 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
PEG/PPG-17/6 COPOLYMER (UNII: P5QZM4T259)  
Glycerin (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83071-010-021 in 1 CARTON10/01/2022
1NDC:83071-010-01120 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other10/01/2022
Labeler - NATURECELL CO., LTD. (689282572)
Registrant - NATURECELL CO., LTD. (689282572)
Establishment
NameAddressID/FEIBusiness Operations
Cosmax, Inc.689049693manufacture(83071-010)

Revised: 11/2022
Document Id: fc23644d-c3a7-4d8f-a395-89dd4d313399
Set id: 921e5fd1-276c-4a2f-9161-97564424df24
Version: 1
Effective Time: 20221107
 
NATURECELL CO., LTD.