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
Active ingredient(s) | Strength |
---|---|
SODIUM FLUORIDE | .24 % |