DR.JUCRE REBIRTH ACTIVATING TONER- betaine 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

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

Image of carton

DR.JUCRE REBIRTH ACTIVATING TONER 
betaine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83071-020
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Betaine (UNII: 3SCV180C9W) (BETAINE - UNII:3SCV180C9W) Betaine0.001 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Triethylhexanoin (UNII: 7K3W1BIU6K)  
Glycerin (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83071-020-021 in 1 CARTON10/01/2022
1NDC:83071-020-01150 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(83071-020)

Revised: 11/2022
Document Id: ff0ae282-1f6c-441a-a7dd-863b46931dc2
Set id: 7f333594-d672-4259-83ae-5d591e620f0d
Version: 1
Effective Time: 20221107
 
NATURECELL CO., LTD.