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ULTRAPLAST ALGINATE STYPTIC GAUZE 5.5 % — DIN 00206946

CALCIUM ALGINATE : 5.5 % SODIUM ALGINATE : 4 % DOMIPHEN BROMIDE : .15 % · WALLACE, CAMERON AND COMPANY LTD. · DRESSING · wholesale supply in Canada

Health Canada status: CANCELLED POST MARKET

What is ULTRAPLAST ALGINATE STYPTIC GAUZE?

ULTRAPLAST ALGINATE STYPTIC GAUZE 5.5 % contains CALCIUM ALGINATE : 5.5 % SODIUM ALGINATE : 4 % DOMIPHEN BROMIDE : .15 %. It is listed in the Health Canada Drug Product Database under DIN 00206946, held by WALLACE, CAMERON AND COMPANY LTD., supplied as DRESSING for TOPICAL administration. Health Canada currently lists it as cancelled post market, status dated 20-Sep-1996. This Drug Identification Number is no longer authorized for sale in Canada, so Nexara does not supply it. The record is kept here because buyers still meet the number on old formularies, purchase orders and tender documents; Nexara can help identify an authorized alternative.

How is it supplied and stored?

Pack configuration, storage class and the handling constraints that drive cold-chain planning. One DIN can cover more than one pack size, and the pack — not the DIN — is what gets priced, shipped and invoiced.

Strength on the label5.5 %
Dosage formDRESSING
RouteTOPICAL

Pack detail is kept as a regulatory record. This DIN is no longer authorized for sale in Canada, so Nexara does not quote this pack.

Substance and classification

Active substanceLocal Hemostatics
ATC codeB02BC
AHFS class84:04.92
Biosimilar biologicNo

Health Canada record and identifiers

The regulatory facts straight from the Drug Product Database, plus every identifier form Nexara accepts on a purchase order. A DIN written without its leading zeros is the commonest reason an order line fails to match.

DIN (8-digit, as used in ordering)00206946
DIN (unpadded, as printed on some documents)206946
Brand nameULTRAPLAST ALGINATE STYPTIC GAUZE
Generic / active ingredientCALCIUM ALGINATE : 5.5 % SODIUM ALGINATE : 4 % DOMIPHEN BROMIDE : .15 %
Market authorization holderWALLACE, CAMERON AND COMPANY LTD.
Health Canada scheduleNON-PRESCRIPTION DRUGS
ATC codeB02BC
ATC anatomical main groupB — Blood and blood-forming organs
ATC therapeutic subgroupB02BC
Current statusCANCELLED POST MARKET
Status date20-Sep-1996
Original market date1969-12-31 00:00:00
Status sourceLive Health Canada DPD sync

Verify on the primary sources

Health Canada DPD record

What can be used instead?

Alternatives on every axis a buyer actually considers — the same molecule in another presentation, the same class, an adjacent class, or a fixed-dose combination. Every row is led by the marketed DIN count, because that is what can be bought this week.

2 · Same class — other molecules in ATC B02BC

MoleculeCanadian brandsDINsMarketedSourceable
CombinationsARTISS · EVICEL · QUIXIL · TACHOSIL · +3 more125Yes
EpinephrineADRENALIN TOPICAL SOLUTION11Yes
ThrombinTHROMBINAR PWS 5000UNIT/VIAL · THROMBOGEN · THROMBOGEN SPRAY KIT · THROMBOSTAT 10000UNITS · +2 more90Not in Canada
Local HemostaticsULTRAPLAST ALGINATE STYPTIC GAUZE10Not in Canada

A molecule with zero marketed DINs cannot be sourced domestically, however many approvals it holds — if one of these sits on a formulary or in an older protocol, that is the line to check.

3 · Adjacent classes in ATC B02B

ATC subgroupMoleculesDINsMarketed
B02BDCatridecacog · Coagulation Factor Ix · Coagulation Factor Ix, Ii, Vii And X In Comb · Coagulation Factor Viia · Coagulation Factor Viii · +8 more21673
B02BXAvatrombopag · Concizumab · Eltrombopag · Emicizumab · Fostamatinib · +1 more2315
B02BAPhytomenadione52
B02BBFibrinogen, Human22

4 · Fixed-dose combinations with Canadian supply

ProductActive ingredientsHolderStatusDIN
ADYNOVATEANTIHEMOPHILIC FACTOR (RECOMBINANT), PEGYLATED : 1000 UNITTAKEDA CANADA INCMARKETED02498588
ALPROLIXRECOMBINANT HUMAN COAGULATION FACTOR IX, FC FUSION PROTEIN : 500 UNITSANOFI-AVENTIS CANADA INCMARKETED02422913
ALTUVIIIO*ANTIHEMOPHILIC FACTOR VIII (RECOMBINANT, BDD), FC-VWF-XTEN FUSION PROTEIN : 4000 UNITSANOFI-AVENTIS CANADA INCMARKETED02448157
ELOCTATEANTIHEMOPHILIC FACTOR (RECOMBINANT BDD), FC FUSION PROTEIN : 500 UNITSANOFI-AVENTIS CANADA INCMARKETED02430304
ESPEROCTANTIHEMOPHILIC FACTOR VIII (RECOMBINANT, B-DOMAIN TRUNCATED), PEGYLATED : 2000 UNITNOVO NORDISK CANADA INCMARKETED02490099
JIVIANTIHEMOPHILIC FACTOR (RECOMBINANT, B-DOMAIN DELETED, PEGYLATED) : 1000 UNITBAYER INCMARKETED02481774
REBINYNCOAGULATION FACTOR IX (RECOMBINANT), PEGYLATED : 3000 UNITNOVO NORDISK CANADA INCMARKETED02532964

Not clinical advice. These tables describe what can be supplied in Canada, not what should be prescribed. Substitution within or across classes is a prescriber and pharmacist decision, and interchangeability is determined provincially.

Can this still be bought in Canada?

No. This Drug Identification Number is cancelled post market in Health Canada's Drug Product Database, so the product is no longer authorized for sale in Canada and Nexara does not supply it. This page is kept as a regulatory record.

If you are looking for a current equivalent, the alternatives above list every product sharing this therapeutic class, with the marketed ones first. Ask us to source an alternative

Ordering questions

Who can buy this from Nexara?

Licensed entities only. Nexara holds Health Canada establishment licence DEL 3-002896-A and ships only to a licensed address. Patients and unlicensed buyers are routed to a partner pharmacy.

Is there a minimum order?

Yes, set per product line and per pack multiple rather than on the order total, so you are never asked to buy a part-pack. The minimum for this line is confirmed with your quote.

What is the lead time?

Confirmed per order at quotation, and it depends on current stock position and whether the product is in shortage.

Why is there no price on this page?

Nexara quotes a delivered Canadian price per order, against a verified licence. Foreign list prices are published on incompatible bases and are not a guide to what any buyer can obtain here, so this page shows which markets list the molecule and on what basis, and nothing more.

Can Nexara supply this for a clinical trial?

Yes — comparator and background-therapy supply, including sourcing from other markets where a Canadian pack will not satisfy the protocol. Clinical trial supply.

Sources and disclaimer

Product data sourced from the Health Canada Drug Product Database. Health Canada status reconciled against the live DPD sync. Last reviewed 10 Sep 2026.

Nothing on this page is medical advice. Nexara Health is a licensed wholesale distributor and supplies licensed entities only; consumer orders are routed to a partner pharmacy. Alternatives tables describe supply, not clinical equivalence.

Health Canada Drug Product Database (DPD), DIN 00206946. Last reviewed 2026-09-10. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.