Product information

From Health Canada

Current status:

Cancelled Post Market

Current status date:

1996-09-09

Original market date: See footnote 1

1992-12-31

Product name:

INTERPLAK DEN GEL W FLUORIDE 0.24%

DIN:

01942840 Electronic product monograph is not available

Company:

BAUSCH & LOMB CANADA INC.
1400 North Goodman Street
Rochester
New York
United States 14609

Class:

Human

Dosage form(s):

Gel

Route(s) of administration:

Dental

Number of active ingredient(s):

1

Schedule(s):

OTC

 

American Hospital Formulary Service (AHFS): See footnote 3

34:00.00 

Anatomical Therapeutic Chemical (ATC): See footnote 4

A01AA01 SODIUM FLUORIDE

Active ingredient group (AIG) number:See footnote5

0107147004

List of active ingredient(s)
Active ingredient(s) Strength
SODIUM FLUORIDE .24 %
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