XIMONTH QUICK ESSENCE- salicylic acid liquid

XIMONTH Quick Essence by

Drug Labeling and Warnings

XIMONTH Quick Essence by is a Otc medication manufactured, distributed, or labeled by Shantou Ximonth Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Witch Hazel Extract、Peppermint Extract、Tea Tree Oil

Purpose

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

Use

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

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

Discontinue use if signs of imitation or rash occur

Stop Use

Discontinue use if signs of imitation or rash occur

KEEP OUT OF REACH OF CHILDREN

Please keep out of reach of children. Do not swallow

STORAGE AND HANDLING

Store in a cool and dry place.

INACTIVE INGREDIENT

Purified Water、Salicylic Acid

INDICATIONS & USAGE

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

1. After cleansing or soaking feet.

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

XIMONTH QUICK ESSENCE 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84989-012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TEA TREE OIL (UNII: VIF565UC2G) (TEA TREE OIL - UNII:VIF565UC2G)	TEA TREE OIL	0.04 mg  in 20 mg
PEPPERMINT (UNII: V95R5KMY2B) (PEPPERMINT - UNII:V95R5KMY2B)	PEPPERMINT	0.1 mg  in 20 mg
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	WITCH HAZEL	0.6 mg  in 20 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	19.1 mg  in 20 mg
SALICYLIC ACID (UNII: O414PZ4LPZ)	0.16 mg  in 20 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84989-012-01	20 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	10/30/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	10/30/2025

Labeler - Shantou Ximonth Biotechnology Co., Ltd. (457811606)

Registrant - Shantou Ximonth Biotechnology Co., Ltd. (457811606)

Establishment
Name	Address	ID/FEI	Business Operations
Shantou Ximonth Biotechnology Co., Ltd.		457811606	manufacture(84989-012)