Drug Facts

Active ingredient

Sodium Fluoride 0.02% (0.01% w/v fluoride ion)

Purpose

Anticavity

Use

Aids in the prevention of dental cavities

Warning

Keep out of reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

Adults and children 6 years & older: Use twice a day after brushing your teeth with a toothpaste.
Vigorously swish the 10 mL (2 teaspoonfuls) of rinse between your teeth for 1 minute and then spit out.
Do not swallow the rinse.
Do not eat or drink for 30 minutes after rinsing.
Instruct children under 12 years of age in good rinsing habits (to minimize swallowing).
Supervise children as necessary until capable of using without supervision.
Children under 6 years of age: Consult a dentist or doctor.

Inactive ingredients

water, glycerin, propylene glycol, polysorbate 80, benzoic acid, flavor, saccharin, sodium benzoate, phosphoric acid, disodium phosphate, yellow 5, blue 1

Questions?

1-800-862-7442

DISTR. BY PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 1000 mL Bottle Label

Strong Mint

FLEX YOUR

freshness™

Scope®

ANTICAVITY FLUORIDE MOUTHWASH

STAY STRONG™

plus enamel protection

SEE BACK FOR IMPORTANT INGREDIENT INFORMATION

IMPORTANT: Read directions for proper use.

Kills 99%

of bad breath bacteria*

FORTIFIES ENAMEL with fluoride

1L (33.8 FL OZ)

Scope Stay Strong

SCOPE STAY STRONG
sodium fluoride rinse

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69423-859
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.02 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
BENZOIC ACID (UNII: 8SKN0B0MIM)
PHOSPHORIC ACID (UNII: E4GA8884NN)
WATER (UNII: 059QF0KO0R)
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
BASIC BLUE 1 (UNII: 92N74OA24D)
BASIC YELLOW 5 (UNII: 07BP340B4T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLOXAMER 407 (UNII: TUF2IVW3M2)
ALCOHOL (UNII: 3K9958V90M)
SUCRALOSE (UNII: 96K6UQ3ZD4)

Product Characteristics
Color	green	Score
Shape		Size
Flavor	MINT	Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69423-859-33	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/24/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M021	01/24/2022

Labeler - The Procter & Gamble Manufacturing Company (004238200)

Name	Address	ID/FEI	Business Operations
Establishment
THE PROCTER & GAMBLE MANUFACTURING COMPANY		005279245	manufacture(69423-859) , pack(69423-859)

Name	Address	ID/FEI	Business Operations
Establishment
Merck KGaA		342249299	api manufacture(69423-859)

Name	Address	ID/FEI	Business Operations
Establishment
SUNLIT FLUO & CHEMICAL CO., LTD. CHUNG-LI FACTORY		658870890	api manufacture(69423-859)