PREMIUM NATURAL- premium natural toothpaste with hydroxyapatite paste

Premium Natural by

Drug Labeling and Warnings

Premium Natural 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,Hydroxyapatite,Cellulose Gum,Cocos Nucifera (Coconut) 0il,Sorbitol,Menthol

Purpose section

PRO MINERALIZER FORNATURALLY WHITER TEETH

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 you experience 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.

dosage

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PREMIUM NATURAL 
premium natural toothpaste with hydroxyapatite paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84732-073
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM SILICATE (UNII: T1FAD4SS2M) (ALUMINUM SILICATE - UNII:T1FAD4SS2M)	ALUMINUM SILICATE	1 mg  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CELLULOSE GUM (UNII: K679OBS311)
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
MENTHOL (UNII: L7T10EIP3A)
COCOS NUCIFERA (COCONUT) OIL (UNII: Q9L0O73W7L)
HYDROXYAPATITE (UNII: 91D9GV0Z28)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84732-073-01	100 g in 1 TUBE; Type 0: Not a Combination Product	10/30/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M021	10/30/2024

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

Establishment
Name	Address	ID/FEI	Business Operations
Dongguan Haiyi Technology Co.,Ltd.		722030807	manufacture(84732-073)