UNIVERSAL ADVANCED WHITENING ANTI-CAVITY FLUORIDE- sodium monofluorophosphate paste 
Universal Distribution Center LLC

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UNIVERSAL ADVANCED WHITENING ANTI-CAVITY FLUORIDE TOOTHPASTE

Active Ingredient

Sodium Monofluorophosphate  0.76%

(1000 ppm)

Purpose

Anticavity toothpaste

Uses

Warning

When using this product

Stop and ask a dentist

Sensitivity teeth may indicate a serious problem that may need prompt care by a dentist.

Keep out of reach of children

Directions

Children under 12 years of age: Consult a dentist or doctor

Other information

Inactive Ingredients

Calcium carbonate, Water, Glycerine, Silica, Sodium Lauryl sulphate, Sorbitol, Xanthan gum, Sodium saccharine, Sodium benzoate, Sodium carboxy methyl cellulose, Flavor and FD&C blue #1

PRINCIPAL DISPLAY PANEL

UNIVERSAL ADVANCED WHITENING ANTI-CAVITY FLUORIDE TOOTHPASTE

label

UNIVERSAL ADVANCED WHITENING ANTI-CAVITY FLUORIDE 
sodium monofluorophosphate paste
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52000-112
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.76 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CALCIUM CARBONATE (UNII: H0G9379FGK)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SORBITOL (UNII: 506T60A25R)  
XANTHAN GUM (UNII: TTV12P4NEE)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52000-112-01181 g in 1 TUBE; Type 0: Not a Combination Product05/30/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02105/30/2020
Labeler - Universal Distribution Center LLC (019180459)

Revised: 11/2023
Document Id: e3086345-3da8-4262-9854-15ab1e031e58
Set id: 879dfaf0-27c8-41a3-8d01-a1c3eec9edfc
Version: 2
Effective Time: 20231115
 
Universal Distribution Center LLC