UNIDENTAL ALL CARETOOTHPASTE- sodium monofluorophosphate, cetylpyridinium chloride, potassium nitrate paste, dentifrice 
Unimed Pharmaceuticals, Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Drug Facts

Sodium monofluorophosphate, Cetylpyridinium chloride, Potassium nitrate

Sodium benzoate, Glycerin, Glycyrrhizin acid, Sodium
Copper Chlorophyllin, Sodium lauroyl sarcosinate, Menthol,
Myrrh tincture, Amorphous sorbitol solution(70%),
Saccharin sodium hydrate, Titanium dioxide, Sulfur, Sesin
Ext., Sage Ext., Mugwort Ext., Ascorbic acid, Titrated Ext.
of the unsaponifiable fraction of Zea mays L., Grapefruit
Seed Ext., Xylitol, Purified water, Carboxymethyl Cellulose
sodium, Chmomilla Extract, Bicarbonate sodium, Tocopheryl
acetate, Polyethylene glycol 1500, Propolis Ext.,
Pyrophosphate sodium, Pyridoxine Hydrochloride,
Hydroxyapatite, TIXOSIL 43K, Fragrance

■ Prevention and reduction of tooth pain
■ Protection of sensitive teeth (tooth pain)
■ Tooth decay prevention
■ Dental plaque removal (anti-plaque)
■ Prevention of gingivitis and periodontitis
■ Keeping teeth white and strong
■ Keeping the inside of the mouth clean
■ Aesthetic effect

keep out of reach of the children

Brush your teeth with a suitable amount

■ This toothpaste contains 1,000 ppm of fluoride
■ When used for children under the age of 6, use a very
small amount of toothpaste while teaching them not to
suck or swallow it
■ If a large amount is swallowed by a child under the age
of 6, consult a doctor or a dentist immediately
■ Keep out of reach of children under the age of 6

dental use only

label

UNIDENTAL ALL CARETOOTHPASTE 
sodium monofluorophosphate, cetylpyridinium chloride, potassium nitrate paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73669-012
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844) POTASSIUM NITRATE3.75 g  in 100 g
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.76 g  in 100 g
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) (CETYLPYRIDINIUM - UNII:CUB7JI0JV3) CETYLPYRIDINIUM CHLORIDE0.3 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73669-012-01100 g in 1 TUBE; Type 0: Not a Combination Product04/20/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/20/2023
Labeler - Unimed Pharmaceuticals, Inc. (689852052)
Registrant - Unimed Pharmaceuticals, Inc. (689852052)
Establishment
NameAddressID/FEIBusiness Operations
Unimed Pharmaceuticals, Inc.689852052label(73669-012) , manufacture(73669-012) , pack(73669-012)

Revised: 4/2023
Document Id: f9bf6820-2a0f-896e-e053-6394a90ae14c
Set id: f9bf72cb-56af-a128-e053-6394a90a3cb8
Version: 1
Effective Time: 20230420
 
Unimed Pharmaceuticals, Inc.