Label: EQUATE PRO-ADVANCED TP EQUATE PRO-ADVANCED TP- stannous fluoride paste, dentifrice
- NDC Code(s): 79903-281-70
- Packager: Walmart Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 18, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
Directions adults and children 12 years of age and older: apply at least a 1-inch strip of the product onto a soft bristle toothbrush • brush teeth thoroughly for at least one 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 years of age: Consult a dentist
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
EQUATE PRO-ADVANCED TP EQUATE PRO-ADVANCED TP
stannous fluoride paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-281 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STANNOUS FLUORIDE (UNII: 3FTR44B32Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 0.16 g in 100 g Inactive Ingredients Ingredient Name Strength SACCHARIN SODIUM (UNII: SB8ZUX40TY) ZINC LACTATE (UNII: 2GXR25858Y) GLYCERIN (UNII: PDC6A3C0OX) POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ) XANTHAN GUM (UNII: TTV12P4NEE) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) WATER (UNII: 059QF0KO0R) CARRAGEENAN (UNII: 5C69YCD2YJ) HYDRATED SILICA (UNII: Y6O7T4G8P9) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L) SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS (UNII: SX01TZO3QZ) POVIDONE (UNII: FZ989GH94E) SODIUM GLUCONATE (UNII: R6Q3791S76) Product Characteristics Color blue (light blue to green, with silver flecks) Score Shape Size Flavor MINT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-281-70 1 in 1 CARTON 12/18/2024 1 144 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 12/18/2024 Labeler - Walmart Inc. (051957769) Registrant - Lornamead (080046418) Establishment Name Address ID/FEI Business Operations Lornamead 080046418 manufacture(79903-281) , pack(79903-281)
