FDA.reportPublic FDA data

XIMONTH Quick Essence

Manufacturer
Shantou Ximonth Biotechnology Co., Ltd.
Effective date
2025-11-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:18:28

Label at a glance#

ProductXIMONTH Quick Essence
Active ingredientTEA TREE OIL, PEPPERMINT, WITCH HAZEL
Label structure12 sections

Storage and handling

Store in a cool and dry place.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Witch Hazel Extract、Peppermint Extract、Tea Tree Oil

Purpose

OTC - PURPOSE SECTION

Safe for all skin types, the ingredients are effective in minimizing diffusion while keeping the skin free from damage.

Use

OTC - WHEN USING SECTION

1. After cleansing or soaking feet

2. Use the brush of this product to apply appropriate amount of this product to the affected area

Warnings

WARNINGS SECTION

Please clean your hands before use to ensure the best results from the product. Discontinue use if signs of irritation or rash occur.Store in a cool and dry place.

Do not use

OTC - DO NOT USE SECTION

Discontinue use if signs of imitation or rash occur

Stop Use

OTC - STOP USE SECTION

Discontinue use if signs of imitation or rash occur

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Please keep out of reach of children. Do not swallow

STORAGE AND HANDLING SECTION

Store in a cool and dry place.

INACTIVE INGREDIENT SECTION

Purified Water、Salicylic Acid

INDICATIONS & USAGE SECTION

1. After cleansing or soaking feet.

2. Use the brush of this product to apply appropriate amount of this product to the affected area.

DOSAGE & ADMINISTRATION SECTION

1. After cleansing or soaking feet.

2. Use the brush of this product to apply appropriate amount of this product to the affected area.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
PEPPERMINT Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84989-012-01XIMONTH Quick Essence20 mg in 1 BOTTLE, GLASSLIQUID202

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84989-01284989-012-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
TEA TREE OILVIF565UC2GACTIB
WATER059QF0KO0RIACT
PEPPERMINTV95R5KMY2BACTIB
SALICYLIC ACIDO414PZ4LPZIACT
WITCH HAZEL101I4J0U34ACTIB

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
XIMONTH Quick EssenceSALICYLIC ACIDShantou Ximonth Biotechnology Co., Ltd.4256f607-c9cf-cd0f-e063-6394a90a54872025-11-26WarningsExact identifier
ndc (package): 84989-012-01
ndc (product): 84989-012
ndc11 (package): 84989001201
spl id: 448b7147-f046-c50a-e063-6294a90a2f75
spl set id: 4256f607-c9cf-cd0f-e063-6394a90a5487

Reported adverse events (FAERS/openFDA)#

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