Label: CREST PRO-HEALTH- stannous fluoride paste, dentifrice
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NDC Code(s):
37000-888-01,
37000-888-03,
37000-888-04,
37000-888-06, view more37000-888-09, 37000-888-12, 37000-888-24
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 17, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Purposes
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Uses
- aids in the prevention of cavities
- helps prevent gingivitis
- helps interfere with the harmful effects of plaque associated with gingivitis
- helps control plaque bacteria that contribute to the development of gingivitis
- builds increasing protection against painful sensitivity of the teeth to cold, heat, acids, sweets or contact
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Warnings
When using this product do not use for sensitivity longer than four weeks unless recommended by a dentist.
Stop use and ask a dentist if the sensitivity problem persists or worsens. Sensitive teeth may indicate a serious problem that may need prompt care.
Keep out of reach of children. If more than used for brushing is accidentally swallowed, get medical help or
contact a Poison Control Center right away.
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Directions
- adults and children 12 yrs. & older: apply at least a 1-inch strip of the product onto a soft bristle toothbrush. Brush teeth thoroughly for at least 1 minute twice a day (morning and evening) or as recommended by a dentist. Make sure to brush all sensitive areas of the teeth.
- do not swallow
- children under 12 yrs.: ask a dentist
- KEEP OUT OF REACH OF CHILDREN
- Other information
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CREST PRO-HEALTH
stannous fluoride paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37000-888 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STANNOUS FLUORIDE (UNII: 3FTR44B32Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 1.4 mg in 1 g Inactive Ingredients Ingredient Name Strength STANNOUS CHLORIDE (UNII: 1BQV3749L5) WATER (UNII: 059QF0KO0R) HYDRATED SILICA (UNII: Y6O7T4G8P9) CARRAGEENAN (UNII: 5C69YCD2YJ) SODIUM GLUCONATE (UNII: R6Q3791S76) XANTHAN GUM (UNII: TTV12P4NEE) ZINC CITRATE (UNII: K72I3DEX9B) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SORBITOL (UNII: 506T60A25R) SODIUM HYDROXIDE (UNII: 55X04QC32I) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SUCRALOSE (UNII: 96K6UQ3ZD4) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Product Characteristics Color blue Score Shape Size Flavor SPEARMINT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37000-888-04 1 in 1 CARTON 12/19/2016 1 130 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:37000-888-06 1 in 1 CARTON 12/19/2016 2 178 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:37000-888-03 1 in 1 CARTON 12/19/2016 3 93 g in 1 TUBE; Type 0: Not a Combination Product 4 NDC:37000-888-09 2 in 1 CELLO PACK 12/19/2016 4 1 in 1 CARTON 4 130 g in 1 TUBE; Type 0: Not a Combination Product 5 NDC:37000-888-01 1 in 1 CARTON 12/19/2016 5 24 g in 1 TUBE; Type 0: Not a Combination Product 6 NDC:37000-888-12 3 in 1 CELLO PACK 12/19/2016 6 1 in 1 CARTON 6 130 g in 1 TUBE; Type 0: Not a Combination Product 7 NDC:37000-888-24 1 in 1 CARTON 12/19/2016 7 79 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 12/19/2016 Labeler - The Procter & Gamble Manufacturing Company (004238200)