Active Ingredient
Salicylic acid 0.25%
Zenotri Scalp Essence
FDA Label NDC 81817-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Chromach Co., Ltd. for the product Zenotri Scalp Essence (NDC 81817-101). 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 ingredient, purpose, use, warnings, keep out of reach of children, directions, inactive ingredients, zenotri scalp essence, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antidandruff
Use
For the relief of the symptoms of dandruff
Warnings
For external use only
When using this product avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.
Stop use and ask a doctor if condition worsens or does not improve after regular use of this product as directed
Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away
Directions
For best results use at least twice a week or as directed by a doctor.
Apply the essence to all areas where trouble such as dandruff and inflammation on the scalp is absorbed.
Inactive Ingredients
Water, Propylene Glycol, Betaine, Ammonium Acryloyldimethyltaurate/VP Copolymer, 1,2-Hexanediol, Caprylyl Glycol, Menthol, Salicylic acid, Disodium EDTA, Panthenol, Arginine, Butylene Glycol, t-Butyl Alcohol, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Isopropyl Myristate, Artemisia Princeps Leaf Extract, Panax ginseng root Extract, Ethylhexylglycerin, Copper Tripeptide-1, Palmitoyl Pentapeptide-4, rh-Oligopeptide-1
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