Label: CREST PRO-HEALTH ADVANCED ANTIBAC PROTECTION- stannous fluoride paste, dentifrice
- NDC Code(s): 69423-820-50
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 18, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Purposes
-
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
- Warning
-
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. of age: ask a dentist - KEEP OUT OF REACH OF CHILDREN
- Other information
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
-
Principal Display Panel - 24 g tube in carton
CREST
PRO-HEALTH
FLUORIDE TOOTHPASTE FOR
ANTICAVITY AND ANTIGINGIVITIS AND SENSITIVE TEETH
NET WT 5.0 OZ (141 g)
… CAVITIES
… GINGIVITIS
… ENAMEL
… SENSITIVITY
… PLAQUE
… TARTAR
… WHITENING
… FRESHENS
BREATHDENTIST DESIGNED
CLINICALLY PROVEN
ADVANCED
ANTIBACTERIAL PROTECTION
MINT BURST
100% WHOLE MOUTH PROTECTION
24 HOUR ANTI-BAC PROTECTION
-
INGREDIENTS AND APPEARANCE
CREST PRO-HEALTH ADVANCED ANTIBAC PROTECTION
stannous fluoride paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-820 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STANNOUS FLUORIDE (UNII: 3FTR44B32Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 1.5 mg in 1 g Inactive Ingredients Ingredient Name Strength SUCRALOSE (UNII: 96K6UQ3ZD4) 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) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) SODIUM CITRATE (UNII: 1Q73Q2JULR) Product Characteristics Color white Score Shape Size Flavor MINT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-820-50 1 in 1 CARTON 12/18/2023 1 141 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 12/18/2023 Labeler - The Procter & Gamble Manufacturing Company (004238200)