HAE YAN TOOTH- precipitated calcium carbonate, aluminum chlorohydroxy allantoinate, aminocaproic acid, dibasic calcium phosphate hydrate paste

Hae Yan Tooth by

Drug Labeling and Warnings

Hae Yan Tooth by is a Otc medication manufactured, distributed, or labeled by WOORILIFE&HEALTH. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

precipitated calcium carbonate, aminocaproic acid, aluminium chlorohydrin allantoinate, dibasic calcium phosphate hydrate

INACTIVE INGREDIENT

d-sorbitol solution, glycerin, silica, roasted salt, xanthan gum, carboxymethylcellulose sodium, sodium lauryl sulfate, grapefruit seed extract, sodium saccharin, xylitol, l-menthol, green tea extract, propolis extract, glycyrrhiza extract, mulberry root extract, peppermint oil, purified water

PURPOSE

aids in the prevention of dental cavities.

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

• Adults and children 2 years of age and older

Brush teeth thoroughly preferably after each meal or at least twice a day or as directed by a dentist or docter.

• Children under 6 years

To minimize swallowing, use a pea-sized amount and supervise brushing until good habits are established.

• Children under 2 years

Consult a dentist or doctor

WARNINGS

1) Be careful not to swallow it, and rinse your mouth thoroughly after use.

2) If any abnormalities such as gum or mouth damage are caused by using this toothpaste, stop using the product and consult a doctor or dentist.

3) For children under 6 years of age, use a small amount of pea toothpaste per serving and use it under the supervision of a guardian to avoid sucking or swallowing.

4) If a child under 6 years of age swallows a large amount, consult a doctor or dentist immediately.

5) Keep out of reach of children under 6 years old.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAE YAN TOOTH 
precipitated calcium carbonate, aluminum chlorohydroxy allantoinate, aminocaproic acid, dibasic calcium phosphate hydrate paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73065-0004
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMINOCAPROIC ACID (UNII: U6F3787206) (AMINOCAPROIC ACID - UNII:U6F3787206)	AMINOCAPROIC ACID	0.09 g  in 100 g
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) (ANHYDROUS DIBASIC CALCIUM PHOSPHATE - UNII:L11K75P92J)	DIBASIC CALCIUM PHOSPHATE DIHYDRATE	0.09 g  in 100 g
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CATION	37 g  in 100 g
ALCLOXA (UNII: 18B8O9DQA2) (ALCLOXA - UNII:18B8O9DQA2)	ALCLOXA	0.09 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
XYLITOL (UNII: VCQ006KQ1E)
LEVOMENTHOL (UNII: BZ1R15MTK7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73065-0004-1	130 g in 1 TUBE; Type 0: Not a Combination Product	05/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/25/2020

Labeler - WOORILIFE&HEALTH (694860803)

Registrant - WOORILIFE&HEALTH (694860803)

Establishment
Name	Address	ID/FEI	Business Operations
WOORILIFE&HEALTH		694860803	manufacture(73065-0004)