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UPTITE DIN 02238860

Status: Cancelled (Unreturned Annual)
Holder: UPTITE COMPANY INC.
Molecule: BENTONITE

Health Canada record

Active ingredient(s)BENTONITE 167 G; KAOLIN 167 G; SODIUM BORATE 13 G
Dosage formPaste
RouteTopical
ScheduleNON-PRESCRIPTION DRUGS
ClassVeterinary
ATC
Original market date01-Oct-1998
Current status date08-Jan-2024
SourceHealth Canada DPD

Establishment licence of the holder

Uptite Company Inc. — licence , not currently licensed, last inspection rating C (2013-02-04).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing BENTONITE

DINProductCompanyFormStrengthStatus
02230242KOOL OUT CLAYFINISH LINE HORSE PRODUCTS, INC.PasteBENTONITE 63.4 MG; KAOLIN 481.3 MG; BORIC ACID 6.7 MGCancelled Post Market
02230184ORIGINAL PREMIUM CLAYFINISH LINE HORSE PRODUCTS, INC.PasteBENTONITE 69.5 MG; KAOLIN 474.9 MG; SALICYLIC ACID 3.4 MG; METHYL SALICYLATE 0.10 MG; BORIC ACID 3.6 MG; EUCALYPTUS OIL 0.10 MG; PEPPERMINT OIL 0.10 MGCancelled Post Market
02025027POULTICE POWDERAUSTIN, DIVISION OF VÉTOQUINOL N.-A. INC.PowderBENTONITE 932.6 MG; METHYL SALICYLATE 15.6 MG; ALUMINUM POTASSIUM SULFATE 17.3 MG; MAGNESIUM SULFATE 34.5 MGCancelled Post Market

International API supply for BENTONITE

1 active FDA Drug Master Files.

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