NDC Code(s) : 52257-1320-1
Packager : ATOMY CO., LTD.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

ATOMY PROPOLIS Sodium Monofluorophosphate, Sodium Fluoride PASTE, DENTIFRICE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52257-1320
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Sodium Monofluorophosphate(UNII: C810JCZ56Q)
(FLUORIDE ION - UNII:Q80VPU408O) 		FLUORIDE ION0.32 g in 200 g
Sodium Fluoride(UNII: 8ZYQ1474W7)
(FLUORIDE ION - UNII:Q80VPU408O) 		FLUORIDE ION0.20 g in 200 g
Inactive Ingredients
Ingredient Name Strength
Silicon dioxide(UNII: ETJ7Z6XBU4)
Sodium pyrophosphate(UNII: O352864B8Z)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:52257-1320-1200 g in 1 CARTON Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part355 02/01/2015

PRINCIPAL DISPLAY PANEL

Image of carton