AMERFRESH TOOTHPOWDER- sodium fluoride powder

Amerfresh Toothpowder by

Drug Labeling and Warnings

Amerfresh Toothpowder by is a Otc medication manufactured, distributed, or labeled by Yangzhou ONE & ONLY Personal Care Products Co., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Sodium Fluoride 0.22%(0.1 w/v Fluoride ion)

Purpose

Anticavity toothpaste

Uses

aids in the prevention of dental cavities.

Warnings

Keep out of the reach of children under 6 years of age. If more than used for brushing is accidently swallowed,get medical help or contact a Poison Control Center immediately.

Keep out of reach of children under 6 years of age.

Directions

For Use:

• Wet toothbrush and dip into powder until brush is fully covered. 
• Brush teeth and gum line for tleast 30 seconds, rinse and spit out thoroughly
• do not swallow .
• supervise children as necessary until capable of useing without supervision
• instruct children under 12 years of age in good brushing and rinsing habits (to minimize swallowing).
• Adults and children 6 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 a physician.
• Children under 6 years of age:do not use unless directed by a doctor or dentist.

INACTIVE INGREDIENT

calcium carbonate, silica,sodium lauryl sulfate, flavor, sodium sacharine, methylisothiazolinone

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AMERFRESH TOOTHPOWDER 
sodium fluoride powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85162-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
POTASSIUM SODIUM SACCHARATE (UNII: 73U34YC90U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85162-007-01	40 in 1 CARTON	08/13/2025
1		454 g in 1 PACKAGE; Type 0: Not a Combination Product
2	NDC: 85162-007-02	4 in 1 CARTON	08/13/2025
2		50 in 1 BOX
2		57 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M021	08/13/2025

Labeler - Yangzhou ONE & ONLY Personal Care Products Co., LTD (458091296)

Registrant - Yangzhou ONE & ONLY Personal Care Products Co., LTD (458091296)

Establishment
Name	Address	ID/FEI	Business Operations
Yangzhou ONE & ONLY Personal Care Products Co., LTD		458091296	manufacture(85162-007)