Mouth Relief Liquid - Shantou South Moon Biotechnology Co., Ltd.

Manufacturer
Shantou South Moon Biotechnology Co., Ltd.
Effective date
2026-04-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:55:12

Label at a glance#

ProductMouth Relief Liquid
Active ingredientMENTHA PIPERITA (PEPPERMINT) LEAF
Label structure12 sections

Storage and handling

Store in a cool and dry place.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

MENTHA PIPERITA (PEPPERMINT) EXTRACT

OTC - PURPOSE SECTION

Natural relief for gum swelling Gentle on inflamed gums Provides soothing care for swollen and redgums

OTC - WHEN USING SECTION

1. Shake well before use 2. Press the spray 1-2 times to spray in the mouth, it is recommended to use 2-3 times a day to achieve better results.

WARNINGS SECTION

Please keep out of reach of children. Do not swallow.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.

OTC - DO NOT USE SECTION

Discontinue use if signs of irritation or rash occur.

OTC - STOP USE SECTION

Discontinue use if signs of irritation or rash occur.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Please keep out of reach of children.

STORAGE AND HANDLING SECTION

Store in a cool and dry place.

INACTIVE INGREDIENT SECTION

AQUA、 GLYCERIN、 GLUCONOLACTONE、 1,2-HEXANEDIOL、 VITAMIN B1、 ALLANTOIN

INDICATIONS & USAGE SECTION

1. Shake well before use 2. Press the spray 1-2 times to spray in the mouth, it is recommended to use 2-3 times a day to achieve better results.

DOSAGE & ADMINISTRATION SECTION

1. Shake well before use 2. Press the spray 1-2 times to spray in the mouth, it is recommended to use 2-3 times a day to achieve better results.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84983-031-01Mouth Relief Liquid25 mg in 1 BOTTLE, PLASTICLIQUID251

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84983-03184983-031-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
508190ae-6314-b522-e063-6394a90a9c38508190ae-6313-b522-e063-6394a90a9c382026-04-28WarningsExact identifier
spl id: 508190ae-6314-b522-e063-6394a90a9c38
spl set id: 508190ae-6313-b522-e063-6394a90a9c38

Reported adverse events (FAERS/openFDA)#

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