NDC Code(s) : 0363-8203-32, 0363-8203-39
Packager : Walgreens

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Walgreens Fluoride PASTE, DENTIFRICE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0363-8203
Route of Administration DENTAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE(UNII: 8ZYQ1474W7)
(FLUORIDE ION - UNII:Q80VPU408O) 		FLUORIDE ION0.24 g in 100 g
Inactive Ingredients
Ingredient Name Strength
GLYCERIN(UNII: PDC6A3C0OX)
SUCRALOSE(UNII: 96K6UQ3ZD4)
SACCHARIN SODIUM(UNII: SB8ZUX40TY)
SORBITOL(UNII: 506T60A25R)
HYDRATED SILICA(UNII: Y6O7T4G8P9)
WATER(UNII: 059QF0KO0R)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
SODIUM PHOSPHATE(UNII: SE337SVY37)
CARBOXYMETHYLCELLULOSE SODIUM(UNII: K679OBS311)
CHLORINE DIOXIDE(UNII: 8061YMS4RM)
SODIUM PHOSPHATE, DIBASIC ANHYDROUS(UNII: 22ADO53M6F)
Product Characteristics
Color white Score
Shape Size
Flavor MINT Imprint Code
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0363-8203-391 in 1 CARTON
1NDC:0363-8203-32198 g in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part355 10/01/2012

PRINCIPAL DISPLAY PANEL

mm1.jpg

Carton label

mm2.jpg

Carton label