Dr.jucre Rebirth Activating Toner Liquid
FDA Label NDC 83071-020

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Naturecell Co., Ltd. for the product Dr.jucre Rebirth Activating Toner (NDC 83071-020). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredients, inactive ingredients, purpose, warnings, keep out of reach of children, uses, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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

* Please review the disclaimer below.