FRESH MINT TEETH WHITENING paste

FRESH MINT TEETH WHITENING by

Drug Labeling and Warnings

FRESH MINT TEETH WHITENING by is a Otc medication manufactured, distributed, or labeled by Dongguan Haiyi Technology Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Silica

Inactive ingredient

Aqua.Cellulose Gum.Mentha Piperita (Peppermint) Extract,Sorbitol,Menthol

Purpose section

Freshens breath, whitens and cleanses.

Warning

1).For external use only, avoid directcontact with eyes, lf you feel any
discomfort, stop using itand wash it with plenty of water. In severe cases,
pleaseseek medical attention in time.
2). Not allowed to be used ondamaged skin,

stop use

This product may cause allergic reactions in asmall number of people.
lf youexperience any discomfort,please stop using it immediately.

not use

Not suitable for use by children, pregnantor breast feeding people.

OUT OF CHILDREN

KEEP THE PRODUCT OUT OF REACH OF CHILDREN to

HOW TO USE

Apply Squeeze a pea-sized amount of toothpaste onto a soft-bristled toothbrush.

Brush: Gently brush your teeth in circular motions for two minutes, ensuring all surfaces are covered

Rinse: Thoroughly rinse your mouth with water after brushing. Avoid swallowing the toothpaste.For best results, brush your teeth twice daily, especially after meals, and consult your dentist regularly.

Dosage

For best results, brush your teeth twice daily, especially after meals, and consult your dentist regularly.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FRESH MINT TEETH WHITENING 
fresh mint teeth whitening paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84732-085
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	1 mg  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
MENTHA PIPERITA (PEPPERMINT) LEAF EXTRACT (UNII: A389O33LX6)
CELLULOSE GUM (UNII: K679OBS311)
MENTHOL (UNII: L7T10EIP3A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84732-085-01	100 g in 1 TUBE; Type 0: Not a Combination Product	11/05/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M021	11/05/2024

Labeler - Dongguan Haiyi Technology Co.,Ltd. (722030807)

Establishment
Name	Address	ID/FEI	Business Operations
Dongguan Haiyi Technology Co.,Ltd.		722030807	manufacture(84732-085)