ZENOTRI Scalp Essence

Manufacturer
CHROMACH Co., Ltd. | SUANN HYANGJANG Co.,LTD
Effective date
2021-05-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:40:21

Label at a glance#

ProductZENOTRI Scalp Essence
Active ingredientSALICYLIC ACID
Label structure8 sections

Dosage and administration

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.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 0.25%

Purpose

OTC - PURPOSE SECTION

Antidandruff

Use

INDICATIONS & USAGE SECTION

For the relief of the symptoms of dandruff

Warnings

WARNINGS SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

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

ZENOTRI Scalp Essence

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

25mL25mL

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d1c9d1af-bddd-448d-86f7-69052b7d5b47Product name120220627
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81817-101-032023-01-30C16284748780-1f386c64a-2ff5-0266-e053-dadaa90a7c1ac231cbcd-4fe5-16ba-e053-2a95a90a2f8d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81817-101-01ZENOTRI Scalp Essence25 mL in 1 TUBEGEL253
81817-101-03ZENOTRI Scalp Essence1 in 1 CARTONGEL13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81817-101ZENOTRI SCALP ESSENCE (SALICYLIC ACID) GEL [CHROMACH CO., LTD.]3Legacy NDC, 2 package rows20210514_c231cbcd-4fe5-16ba-e053-2a95a90a2f8d.zip

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81817-10181817-101-01, 81817-101-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c232dbea-31cc-2092-e053-2a95a90aad3ec231cbcd-4fe5-16ba-e053-2a95a90a2f8d2021-05-13WarningsExact identifier
spl id: c232dbea-31cc-2092-e053-2a95a90aad3e
spl set id: c231cbcd-4fe5-16ba-e053-2a95a90a2f8d

Reported adverse events (FAERS/openFDA)#

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