CREST PRO-HEALTH ADVANCED COMPLETE CARE ANTICAVITY FLUORIDE- sodium fluoride rinse

Crest Pro-Health Advanced Complete Care by

Drug Labeling and Warnings

Crest Pro-Health Advanced Complete Care by is a Otc medication manufactured, distributed, or labeled by The Procter & Gamble Manufacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active ingredient

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

Purpose

Anticavity

Use

Aids in the prevention of dental cavities

Warnings

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 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, flavor, poloxamer 407, cetylpyridinium chloride, sodium saccharin, phosphoric acid, methylparaben, sucralose, propylparaben,
disodium phosphate, blue 1

Questions?

1-800-285-9139

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DISTR. BY
PROCTER & GAMBLE,
CINCINNATI, OH 45202

Crest Pro Heath Advanced Complete Care 1L

Crest

Pro-Health

Anticavity Fluoride Mouthwash

Advanced

Complete Care*

Alchol Free

IMPORTANT: Read directions for proper use.

6 in 1 Benefits

KILLS MILLIONS OF BAD BREATH GERMS

FRESHENS BREATH

2X ENAMEL PROTECTION SYSTEM**
HELPS PREVENT CAVITIES

STRENGTHENS TEETH

100% WHOLE MOUTH CLEAN

CLEAN MINT

1L (33.8 FL OZ)

INGREDIENTS AND APPEARANCE

CREST PRO-HEALTH ADVANCED COMPLETE CARE  ANTICAVITY FLUORIDE
sodium fluoride rinse

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-751
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
METHYLPARABEN (UNII: A2I8C7HI9T)
SUCRALOSE (UNII: 96K6UQ3ZD4)
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
POLOXAMER 407 (UNII: TUF2IVW3M2)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PHOSPHORIC ACID (UNII: E4GA8884NN)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-751-01	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2023
2	NDC: 69423-751-03	3 in 1 CELLO PACK	01/02/2023
2		1000 mL in 1 BOTTLE, PLASTIC; 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	01/02/2023

Labeler - The Procter & Gamble Manufacturing Company (004238200)