DR.JUCRE REBIRTH WHITE BOOSTER- niacinamide liquid

Dr.Jucre Rebirth White Booster by

Drug Labeling and Warnings

Dr.Jucre Rebirth White Booster by is a Otc medication manufactured, distributed, or labeled by NATURECELL CO., LTD., Cosmax, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

DR.JUCRE REBIRTH WHITE BOOSTER 
niacinamide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83071-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	Niacinamide	2.0 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
PEG/PPG-17/6 COPOLYMER (UNII: P5QZM4T259)
Glycerin (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83071-010-02	1 in 1 CARTON	10/01/2022
1	NDC: 83071-010-01	120 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		10/01/2022

Labeler - NATURECELL CO., LTD. (689282572)

Registrant - NATURECELL CO., LTD. (689282572)

Establishment
Name	Address	ID/FEI	Business Operations
Cosmax, Inc.		689049693	manufacture(83071-010)