KILL FIRETOOTHPASTE- sodium fluoride paste

Kill fireToothpaste by

Drug Labeling and Warnings

Kill fireToothpaste by is a Otc medication manufactured, distributed, or labeled by Pharmacal-International. Co., Ltd., KMPHARMACEUTICAL Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Sodium Fluoride 0.02%

Purpose

• Anticavity Toothpaste

Use

• Aids in the prevention of dental cavities

Directions

• Apply appropriate amount on a toothbrush and brush teeth.

Warnings

• Be careful not to swallow. Rinse mouth thoroughly after use.
• If pain occurs when using this product, stop using and consult your dentist.
• For children under 6 years of age, use a pea size amount of toothpaste as recommended by the KFDA. Use under the guidance of a guardian.
• If a child under 6 years old swallows a large amount, consult a physician or dentist immediately.
• Keep out of the reach of children under 6 years old.

Inactive ingredients

Silica,Sorbitol, Tetrasodium Pyrophosphate, Tocopheryl Acetate,
Xylitol, Glucosyl Stevioside, Hydrated Silica, Cellulose Gum, Sodium lauryl Sulfate, Menthol,
Chamomilla Recutita (Matricaria) Extract, Artemisia Princeps Extract, Zingiber Officinale (Ginger) Root Extract,
Melaleuca Alternifolia (Tea Tree) Leaf Oil, Flavor, Gardenia Red, Water

Effect- Efficacy

• Whitens teeth while fighting germs
• Long-lasting freshness and clean mouth feel
• Protects against cavities and bad breath
• Natural brightness of your teeth shines
• Anti plaque
• Helps prevent plaque, gingivitis cavities and gum disease

Product label

INGREDIENTS AND APPEARANCE

KILL FIRETOOTHPASTE 
sodium fluoride paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24765-133
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	SODIUM FLUORIDE	0.02 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
SORBITOL (UNII: 506T60A25R)
XYLITOL (UNII: VCQ006KQ1E)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
MATRICARIA CHAMOMILLA WHOLE (UNII: G0R4UBI2ZZ)
GINGER (UNII: C5529G5JPQ)
TEA TREE OIL (UNII: VIF565UC2G)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 24765-133-01	100 g in 1 TUBE; Type 0: Not a Combination Product	06/15/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/15/2021

Labeler - Pharmacal-International. Co., Ltd. (557805060)

Registrant - Pharmacal-International. Co., Ltd. (557805060)

Establishment
Name	Address	ID/FEI	Business Operations
KMPHARMACEUTICAL Co.,Ltd.		689850153	manufacture(24765-133)