SP8TOOTHPASTE gel, dentifrice

SP8Toothpaste by

Drug Labeling and Warnings

SP8Toothpaste by is a Otc medication manufactured, distributed, or labeled by Shenzhenshishengyakeji Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Lactobacillus Ferment ：36mg in 120g
Sodium Bicarbonate：12mg in 120g
Mentha Piperita (Peppermint) Leaf Extract:12mg in 120g

PURPOSE

FRESHEN THE BREATH.CLEAN THE TEETH.

ASK DOCTOR

Conditon worse or doesnot improve after regular use as directed

DOSAGE & ADMINISTRATION

Take an appropriate amount oftoothpaste on the toothbrush.
Gently brush your teeth in circularmotions frominside to
outside for1-2minutes.Rinse with clean water.

WHEN USING

Gently brush your teeth in circularmotions frominside to
outside for1-2minutes.

WARNINGS

Keep out of reach of children.Avoid direct contact with eyes
Discontinue use if irritation occursStore in a cool and dry place.

INDICATIONS & USAGE

FRESHEN THE BREATH.CLEAN THE TEETH.

KEEP OUT OF REACH OF CHILDREN

Please keep out of reach of children.

INACTIVE INGREDIENT

Glycerin:24mg in 120g
Sodium Lauryl Sulfate:24mg in 120g
Calcium Carbonate:12mg in 120g

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SP8TOOTHPASTE 
sp8toothpaste gel, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84752-022
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LACTOBACILLUS (UNII: 5307V7XW8I) (LACTOBACILLUS - UNII:5307V7XW8I)	LACTOBACILLUS	36 mg  in 120 g
PEPPERMINT (UNII: V95R5KMY2B) (PEPPERMINT - UNII:V95R5KMY2B)	PEPPERMINT	12 mg  in 120 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM LAURYL SULFATE (UNII: 368GB5141J)	24 mg  in 120 g
GLYCERIN (UNII: PDC6A3C0OX)	24 mg  in 120 g

Product Characteristics
Color	purple	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84752-022-01	120 g in 1 BOTTLE; Type 0: Not a Combination Product	11/06/2024	12/31/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	11/06/2024	12/31/2025

Labeler - Shenzhenshishengyakeji Co., Ltd. (619715687)

Registrant - Shenzhenshishengyakeji Co., Ltd. (619715687)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhenshishengyakeji Co., Ltd.		619715687	label(84752-022)