NATURE MINT ANTICAVITY- sodium monofluorophosphate paste, dentifrice 
Bob Barker Company Inc.

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Nature Mint® Anticavity

Drug Facts:

Active ingredient

Sodium Monofluorophosphate - 0.76% (0.1% w/v fluoride ion)

Purpose

Anticavity toothpaste

Use

Helps protect against cavities.

Warnings

Keep out of the reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Adults & Children 6 years of age & older:Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor.
Children 2 to 6 years:Use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing).
Children under 2 years:Ask a dentist or physician.

Inactive Ingredients

Calcium Carbonate, Water, Sorbitol, Glycerin, Sodium Lauryl Sulfate, Hydrated Silica, Cellulose Gum, Flavor, Sodium Saccharin, Tetrasodium Pyrophosphate, Sodium Benzoate

Dist. by Bob Barker Co. Inc. Fuquay-Varina, NC 27526

PRINCIPAL DISPLAY PANEL - 24 GRAM Tube Label

Nature Mint®

ANTICAVITY FLUORIDE TOOTHPASTE

SODIUM MONOFLUOROPHOSPHATE - 0.76%

FRESH MINT FLAVOR

NET WT 0.85 OZ (24 GRAMS)

PRINCIPAL DISPLAY PANEL - 24 GRAM Tube Label
NATURE MINT ANTICAVITY 
sodium monofluorophosphate paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53247-123
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Sodium Monofluorophosphate (UNII: C810JCZ56Q) (Fluoride Ion - UNII:Q80VPU408O) Fluoride Ion7.6 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
Calcium Carbonate (UNII: H0G9379FGK)  
WATER (UNII: 059QF0KO0R)  
Sorbitol (UNII: 506T60A25R)  
Glycerin (UNII: PDC6A3C0OX)  
Sodium Lauryl Sulfate (UNII: 368GB5141J)  
Hydrated Silica (UNII: Y6O7T4G8P9)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM PYROPHOSPHATE (UNII: O352864B8Z)  
Sodium Benzoate (UNII: OJ245FE5EU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53247-123-017.94 g in 1 PACKET; Type 0: Not a Combination Product01/01/2008
2NDC:53247-123-0217 g in 1 TUBE; Type 0: Not a Combination Product01/01/2008
3NDC:53247-123-0324 g in 1 TUBE; Type 0: Not a Combination Product01/01/2008
4NDC:53247-123-0443 g in 1 TUBE; Type 0: Not a Combination Product01/01/2008
5NDC:53247-123-0578 g in 1 TUBE; Type 0: Not a Combination Product01/01/2008
6NDC:53247-123-061 in 1 CARTON01/01/2008
6130 g in 1 TUBE; Type 0: Not a Combination Product
7NDC:53247-123-071 in 1 CARTON01/01/2008
7181 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph drugM02101/01/2008
Labeler - Bob Barker Company Inc. (058525536)

Revised: 10/2023
Document Id: 4916bff5-91eb-4485-ae42-6176834e29da
Set id: 71010575-d0d0-4c36-87f2-92747e6436a4
Version: 2
Effective Time: 20231031
 
Bob Barker Company Inc.