PERIODONTA GEL- glycerin gel

Periodonta Gel by

Drug Labeling and Warnings

Periodonta Gel by is a Otc medication manufactured, distributed, or labeled by Guangdong Ximonth Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

ALOE VERA LEAF EXTRACT、HYALURONIC ACID、ASCORBIC ACID、ACRYLATES/T-BUTYLAMIN OETHYL METHACRYLATE COPOLYMER

Purpose

Reduce gum recession and tooth loss, ard maintan healthy tissue.

Use

1. Clean and dry your teeth withwarm water. 2. Open the cap and apply this product evenly on the tooth surface. 3. Rinse your mouth with water after 30 minutes.

Do not use

Discontinue use if signs of irritation or rash occur.

STOP USE

Discontinue use if signs of irritation or rash occur.

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.

KEEP OUT OF REACH OF CHILDREN

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

STORAGE AND HANDLING

Avoid freezing and excessive heat above 40C (104F) ）

Store in a cool and dry place.

INACTIVE INGREDIENT

GLYCERIN

DOSAGE & ADMINISTRATION

INDICATIONS & USAGE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PERIODONTA GEL 
glycerin gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84660-015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X) (ALOE VERA LEAF - UNII:ZY81Z83H0X)	ALOE VERA LEAF	1 mg  in 4 mg
ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R)	ASCORBIC ACID	0.6 mg  in 4 mg
ACRYLIC ACID (UNII: J94PBK7X8S) (ACRYLIC ACID - UNII:J94PBK7X8S)	ACRYLIC ACID	0.4 mg  in 4 mg

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	1.2 mg  in 4 mg
HYALURONIC ACID (UNII: S270N0TRQY)	0.8 mg  in 4 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84660-015-01	4 mg in 1 BOX; Type 0: Not a Combination Product	09/09/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M022	09/09/2024

Labeler - Guangdong Ximonth Technology Co., Ltd. (699436264)

Registrant - Guangdong Ximonth Technology Co., Ltd. (699436264)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Ximonth Technology Co., Ltd.		699436264	manufacture(84660-015)