CUREFORTE BREATH RESET- mouth spray spray

Cureforte Breath Reset by

Drug Labeling and Warnings

Cureforte Breath Reset by is a Otc medication manufactured, distributed, or labeled by STEEL CITY HEALTH PRIVATE LIMITED, Guangdong Aimu Biological Technology Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INACTIVE INGREDIENT

Aqua, Xylitol, Aloe, Glycerin, Menthol, Sodium Benzoate, Citric acid

INDICATIONS & USAGE

Usage:

For temporary relief of dry mouth
Helps kill germs that cause bad breath
Helps reduce plaque that leads to early gum problems
Freshens breath

WARNINGS

Warnings:

For oral use only.Do not swallow. Not for children under 6 years of age Stop use and
ask a doctor if irritation or discomfort occurs. Keep out of reach of children

PURPOSE

Purpose:

Glycerin – Temporarily relieves dry mouth
-Cetylpyridinium Chloride – Helps reduce germs that cause bad breath and plaque

KEEP OUT OF REACH OF CHILDREN

Warnings: For oral use only.Do not swallow. Not for children under 6 years of age Stop use and
ask a doctor if irritation or discomfort occurs. Keep out of reach of children

DOSAGE & ADMINISTRATION

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CUREFORTE BREATH RESET 
mouth spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85884-025
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) (CETYLPYRIDINIUM - UNII:CUB7JI0JV3)	CETYLPYRIDINIUM CHLORIDE	0.85 mg  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	100 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE (UNII: V5VD430YW9)
AQUA (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
XYLITOL (UNII: VCQ006KQ1E)
MENTHOL (UNII: L7T10EIP3A)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Product Characteristics
Color		Score
Shape		Size
Flavor	MINT	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85884-025-01	35 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M022	08/01/2025

Labeler - STEEL CITY HEALTH PRIVATE LIMITED (874138259)

Registrant - Guangdong Aimu Biological Technology Co., Ltd (712647107)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Aimu Biological Technology Co., Ltd		712647107	manufacture(85884-025)