MOUTH RELIEF LIQUID- glycerin liquid

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

MENTHA PIPERITA (PEPPERMINT) EXTRACT

PURPOSE

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

WHEN USING

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

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.

DO NOT USE

Discontinue use if signs of irritation or rash occur.

STOP USE

Discontinue use if signs of irritation or rash occur.

KEEP OUT OF REACH OF CHILDREN

Please keep out of reach of children.

STORAGE AND HANDLING

Store in a cool and dry place.

INACTIVE INGREDIENT

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

INDICATIONS & USAGE

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

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.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MOUTH RELIEF LIQUID 
glycerin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84983-031
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHA PIPERITA (PEPPERMINT) LEAF (UNII: A389O33LX6) (MENTHA PIPERITA (PEPPERMINT) LEAF - UNII:A389O33LX6)	MENTHA PIPERITA (PEPPERMINT) LEAF	0.075 mg  in 25 mg

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.75 mg  in 25 mg
GLUCONOLACTONE (UNII: WQ29KQ9POT)	0.025 mg  in 25 mg
ALLANTOIN (UNII: 344S277G0Z)	0.005 mg  in 25 mg
THIAMINE (UNII: X66NSO3N35)	0.0125 mg  in 25 mg
1,2-HEXANEDIOL (UNII: TR046Y3K1G)	0.025 mg  in 25 mg
AQUA (UNII: 059QF0KO0R)	24.1075 mg  in 25 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84983-031-01	25 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/28/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	04/28/2026

Labeler - Shantou South Moon Biotechnology Co., Ltd. (457126192)

Establishment
Name	Address	ID/FEI	Business Operations
Shantou South Moon Biotechnology Co., Ltd.		457126192	manufacture(84983-031)