EQUATE PRO-ADVANCED TP EQUATE PRO-ADVANCED TP- stannous fluoride paste, dentifrice

Equate Pro-Advanced TP by

Drug Labeling and Warnings

Equate Pro-Advanced TP by is a Otc medication manufactured, distributed, or labeled by Walmart Inc., Lornamead. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Stannous fluoride 0.454% (0.16% w/v fluoride ion)

INACTIVE INGREDIENT

glycerin, hydrated silica, sodium hexametaphosphate, water, propylene glycol, PEG-8, zinc lactate, flavor, sodium lauryl sulfate, sodium gluconate, sodium saccharin, trisodium phosphate, xanthan gum, PVP, carrageenan, cocamidopropyl betaine, blue 1

PURPOSE

Anticavity, antigingivitis, antisensitivity

INDICATIONS & USAGE

aids in the prevention of cavities

helps prevent gingivitis

helps interfere with the harmful effects of plaque associated with gingivitis

builds increasing protection against painful sensitivity of the teeth to cold, heat, acids, sweets, or contact

WARNINGS

when using this product, if irritation occurs discontinue use.

Stop use and ask a dentist if if the problem persists or worsens. Sensitive teeth may indicate a serious problem that may need prompt care by a dentist. pain/sensitivty still persists after 4 weeks of use.

Keep out of reach or children.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If more than used for brushing is accidentally swallowed, get meedical help or contact a Poison Control Center right away.

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, dentifrice

Product 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)