Otc - Active Ingredient
Active ingredient: WITCH HAZEL 0.1%
Baeknyondongan Treatment
FDA Label NDC 54948-100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Mix & Match Co., Ltd. for the product Baeknyondongan Treatment (NDC 54948-100). 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 otc - active ingredient, inactive ingredient, otc - purpose, warnings, otc - keep out of reach of children, indications & usage, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Inactive ingredients:
Water, Perilla Ocymoides Leaf Extract, Oryza Sativa (Rice) Extract, Butylene Glycol, Glycerin, Steartrimonium Chloride, Cyclopentasiloxane, Dimethiconol, Stearyl Alcohol, Cetyl Alcohol, Polyquaternium-7, Cyclohexasiloxane, Hydroxyethyl cellulose, Perfume, Betaine, Methylparaben, Tocopheryl Acetate, Propylparaben, Methylchloroisothiazolinone, Methylisothiazolinone, Panthenol, Sophora Angustifolia Root Extract, Ubiquinone, Hydrolyzed keratin
Otc - Purpose
Purpose: Skin Protectant
Warnings
Warnings:For external use only.Do not use on wounds of if you are allergic to any ingredients of this product.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children:
Keep away from children.
Indications & Usage
Indication and usage:
Towel dry your hair after shampooing.
Apply adequate amount of treatment to the hair and leave it for 5-10 minutes before rinsing.
Dosage & Administration
Dosage and administration:
Take appropriate amount according to your hair condition and use it every day.
* Please review the disclaimer below.
