Crest Mystic Enchanted Strawberry

Crest Mystic by

Drug Labeling and Warnings

Crest Mystic by is a Otc medication manufactured, distributed, or labeled by The Procter & Gamble Manufacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CREST MYSTIC ENCHANTED STRAWBERRY- sodium fluoride paste, dentifrice 
The Procter & Gamble Manufacturing Company

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Crest Mystic Enchanted Strawberry

Drug Facts

Active ingredient

Sodium fluoride 0.243% (0.15% w/v fluoride ion)

Purpose

Anticavity toothpaste

Use

helps protect against cavities

Warnings

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

If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

• adults and children 2 yrs. & older: brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist
  • do not swallow
  • to minimize swallowing use a pea-sized amount in children under 6
  • supervise children's brushing until good habits are established
• children under 2 yrs.: ask a dentist

Inactive ingredients

sorbitol, water, hydrated silica, sodium lauryl sulfate, trisodium phosphate, sodium phosphate, cellulose gum, flavor, sodium saccharin, carbomer, red 40

Questions?

1-800-594-4158

PRINCIPAL DISPLAY PANEL - 113 g Tube Carton

3+ YRS

mystic

Crest ®

FLUORIDE ANTICAVITY TOOTHPASTE
MAGICAL CAVITY PROTECTION

MADE WITHOUT MICROBEADS, PARABENS, TRICLOSAN

ENCHANTED STRAWBERRY

NET WT 4.0 OZ (113 g)

CREST MYSTIC  ENCHANTED STRAWBERRY
sodium fluoride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37000-978
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	1.5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SORBITOL (UNII: 506T60A25R)
WATER (UNII: 059QF0KO0R)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SODIUM PHOSPHATE (UNII: SE337SVY37)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS (UNII: SX01TZO3QZ)
FD&C RED NO. 40 (UNII: WZB9127XOA)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37000-978-40	1 in 1 CARTON	07/01/2020
1		113 g in 1 TUBE; 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	07/01/2020	06/01/2024

Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 8/2025

Document Id: 3ccfdb02-7c89-8b0d-e063-6294a90a70d9

34390-5

Set id: ab70db04-ad71-9636-e053-2995a90a559c

Version: 7

Effective Time: 20250820

 

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