DR.JUCRE REBIRTH ACTIVATING TONER- betaine liquid

Dr.Jucre Rebirth Activating Toner by

Drug Labeling and Warnings

Dr.Jucre Rebirth Activating Toner 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

Betaine 0.001%

INACTIVE INGREDIENTS

Water, Triethylhexanoin, Glycerin, Hydrogenated Poly(C6-14 Olefin), Butylene Glycol, Human Adipose Derived Stem Cell Conditioned Media, Pentylene Glycol, Alcohol Denat., Steareth-2, Phenoxyethanol, Hydrogenated Lecithin, Algin, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Citrus Grandis (Grapefruit) Peel Oil, Plankton Extract, Hydroxypropyl Cyclodextrin, Thioctic Acid, 1,2-Hexanediol, Tremella Fuciformis (Mushroom) Extract, Potassium Hydroxide

PURPOSE

Skin Protectant

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

■ skin protectant

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 ACTIVATING TONER 
betaine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83071-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Betaine (UNII: 3SCV180C9W) (BETAINE - UNII:3SCV180C9W)	Betaine	0.001 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Triethylhexanoin (UNII: 7K3W1BIU6K)
Glycerin (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83071-020-02	1 in 1 CARTON	10/01/2022
1	NDC: 83071-020-01	150 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(83071-020)