Dr.Jucre Rebirth Activating Toner

Manufacturer: NATURECELL CO., LTD. | Cosmax, Inc.
Effective date: 2022-11-07
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:51:24

Label at a glance#

ProductDr.Jucre Rebirth Activating Toner

Active ingredientBetaine

Label structure10 sections

Indications and uses

■ skin protectant

Dosage and administration

■ Apply an appropriate amount evenly on the skin.

Contacts and useful links#

Websitewww.ibiostar.com

www.ibiostar.com

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Betaine 0.001%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

Skin Protectant

WARNINGS

WARNINGS SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

Uses

INDICATIONS & USAGE SECTION

■ skin protectant

Directions

DOSAGE & ADMINISTRATION SECTION

■ Apply an appropriate amount evenly on the skin.

Other Information

OTHER SAFETY INFORMATION

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

Questions

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
BETAINE Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
d1c9d1af-bddd-448d-86f7-69052b7d5b47	Product name	1	20220627

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
83071-020-01	Dr.Jucre Rebirth Activating Toner	150 mL in 1 BOTTLE	LIQUID	150		1
83071-020-02	Dr.Jucre Rebirth Activating Toner	1 in 1 CARTON	LIQUID	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
83071-020	DR.JUCRE REBIRTH ACTIVATING TONER (BETAINE) LIQUID [NATURECELL CO., LTD.]	1	Current NDC, Legacy NDC, 2 package rows	20221108_7f333594-d672-4259-83ae-5d591e620f0d.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

Dr.Jucre Rebirth Activating Toner
Betaine
Water
Triethylhexanoin
Glycerin

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
83071-020	83071-020-01, 83071-020-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Betaine	3SCV180C9W	ACTIB
Water	059QF0KO0R	IACT
Triethylhexanoin	7K3W1BIU6K	IACT
Glycerin	PDC6A3C0OX	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Dr.Jucre Rebirth Activating Toner	BETAINE	NATURECELL CO., LTD.	7f333594-d672-4259-83ae-5d591e620f0d	2022-11-07	Warnings	Exact identifier ndc (package): 83071-020-02 ndc (package): 83071-020-01 ndc (product): 83071-020 ndc11 (package): 83071002002 ndc11 (package): 83071002001 spl id: ff0ae282-1f6c-441a-a7dd-863b46931dc2 spl set id: 7f333594-d672-4259-83ae-5d591e620f0d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.