DR.LORD GREEN PROPOL TOOTH- silicon dioxide, aminocaproic acid, aluminum chlorohydroxy allantoinate paste, dentifrice

Dr.LORD Green Propol Tooth by

Drug Labeling and Warnings

Dr.LORD Green Propol Tooth by is a Otc medication manufactured, distributed, or labeled by Red 99, EQMAXON Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Silicon Dioxide 17.0%
Aminocaproic Acid 0.1%
Aluminum Chlorohydroxy Allantoinate 0.1%

INACTIVE INGREDIENTS

Liquid sorbitol(Non-crystallising)(70%), Purified Water, Glycerin, Xylitol, Sodium Lauroyl Sarcosinate, Polyethylene Glycol 1500, Carboxymethylcellulose Sodium, Enzymatically Modified Stevia, Methyl parahydroxy benzoate, Mint Flavor EM-17B032, Methol, Mentha Oil, Propolis Extract, PepperMint Flavor EM-16B196, Chitosan, Licorice Extract, Tartrazine

PURPOSE

Anti-plaque
Gum care
Anti-gingivities

WARNINGS

1. Be careful not to swallow, and rinse your mouth thoroughly after use.
2. If abnormalities occur due to the use of this toothpaste, such as gum or mouth damage, stop using it and consult a doctor or dentist.
3. If children under the age of 6 use toothpaste, use a small amount of toothpaste about the size of peas per session, and use it under the guidance of their guardians not to suck or swallow it.
4. If a child under the age of 6 swallows a large amount, consult a doctor or dentist immediately.
5. Keep out of reach of children under the age of 6

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children under the age of 6

Uses

1. Tooth removal (anti- plaque)
2. Prevention of gingivitis
3. Prevention of gum disease

Directions

Put an appropriate amount on your toothbrush and brush your teeth.

Other Information

airtight container
Storage at room temperature (1~30℃)

Questions

Telephone Number : +82-53-802-5560
E-mail : red99cos@gmail.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR.LORD GREEN PROPOL TOOTH 
silicon dioxide, aminocaproic acid, aluminum chlorohydroxy allantoinate paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82656-010
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Silicon Dioxide (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	Silicon Dioxide	17.0 g  in 100 g
Aminocaproic Acid (UNII: U6F3787206) (AMINOCAPROIC ACID - UNII:U6F3787206)	Aminocaproic Acid	0.1 g  in 100 g
ALCLOXA (UNII: 18B8O9DQA2) (ALLANTOIN - UNII:344S277G0Z)	ALCLOXA	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
Sorbitol (UNII: 506T60A25R)
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82656-010-02	1 in 1 CARTON	03/01/2022
1	NDC: 82656-010-01	180 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/01/2022

Labeler - Red 99 (694767263)

Registrant - Red 99 (694767263)

Establishment
Name	Address	ID/FEI	Business Operations
EQMAXON Corp.		557821534	manufacture(82656-010)