NDC Code(s) : 32909-652-02
Packager : E-Z-EM Canada Inc

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

E-Z-Dose with Liquid Polibar PlusBarium Sulfate SUSPENSION
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:32909-652
Route of Administration RECTAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
barium sulfate(UNII: 25BB7EKE2E)
(barium sulfate - UNII:25BB7EKE2E) 		barium sulfate1.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
acacia(UNII: 5C5403N26O)
anhydrous citric acid(UNII: XF417D3PSL)
dimethicone 350(UNII: 2Y53S6ATLU)
dimethicone 1000(UNII: MCU2324216)
hydrochloric acid(UNII: QTT17582CB)
polysorbate 80(UNII: 6OZP39ZG8H)
potassium chloride(UNII: 660YQ98I10)
potassium sorbate(UNII: 1VPU26JZZ4)
water(UNII: 059QF0KO0R)
saccharin sodium(UNII: SB8ZUX40TY)
silicon dioxide(UNII: ETJ7Z6XBU4)
sodium benzoate(UNII: OJ245FE5EU)
carrageenan(UNII: 5C69YCD2YJ)
trisodium citrate dihydrate(UNII: B22547B95K)
sorbitol(UNII: 506T60A25R)
xanthan gum(UNII: TTV12P4NEE)
Product Characteristics
Color WHITE Score
Shape Size
Flavor VANILLA Imprint Code
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:32909-652-026 in 1 PACKAGE
1650 mL in 1 BOTTLE, DISPENSING Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
Unapproved drug other 11/01/1984

PRINCIPAL DISPLAY PANEL

E-Z-Dose with Liquid Polibar Plus - Package

NDC: 32909-652-02

package label