NDC Code(s) : 67694-090-01
Packager : Dent-Aids

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Up and Up Anticavity Toothpaste Whitening Plus Mouthwash Sodium Fluoride PASTE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:67694-090
Route of Administration DENTAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Sodium Fluoride(UNII: 8ZYQ1474W7)
(Fluoride Ion - UNII:Q80VPU408O) 		Sodium Fluoride2.43 mg in 1 g
Inactive Ingredients
Ingredient Name Strength
SORBITOL(UNII: 506T60A25R)
WATER(UNII: 059QF0KO0R)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
POLYETHYLENE GLYCOL 300(UNII: 5655G9Y8AQ)
SODIUM LAURYL SULFATE(UNII: 368GB5141J)
ALCOHOL(UNII: 3K9958V90M)1.14 mg in 1 g
XANTHAN GUM(UNII: TTV12P4NEE)
CARBOMER 934(UNII: Z135WT9208)
SODIUM BENZOATE(UNII: OJ245FE5EU)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
SODIUM PYROPHOSPHATE(UNII: O352864B8Z)
SACCHARIN SODIUM(UNII: SB8ZUX40TY)
TRICLOSAN(UNII: 4NM5039Y5X)
FD&C BLUE NO. 1(UNII: H3R47K3TBD)
Product Characteristics
Color green Score
Shape Size
Flavor MINT Imprint Code
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:67694-090-01181.4 g in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH DRUG PRODUCT MANUFACTURED EXCLUSIVELY FOR PRIVATE LABEL DISTRIBUTOR 05/31/2011

PRINCIPAL DISPLAY PANEL

Image of Container