Bismuth subnitrate 20% Iodoform 40% paste impregnated gauze dressing 1.25cm x 100cm

Main information

  • Trade name:
  • Bismuth subnitrate 20% Iodoform 40% paste impregnated gauze dressing 1.25cm x 100cm
  • Dosage:
  • 400mg/ 1gram ; 200mg/ 1gram
  • Pharmaceutical form:
  • Impregnated dressing
  • Administration route:
  • Cutaneous
  • Class:
  • No Controlled Drug Status
  • Prescription type:
  • Valid as a prescribable product
  • Medicine domain:
  • Humans
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • Bismuth subnitrate 20%  Iodoform 40% paste impregnated gauze dressing 1.25cm x 100cm
    United Kingdom
  • Language:
  • English

Therapeutic information

  • Product summary:
  • BNF: ; GTIN: 5026468000074

Status

  • Source:
  • eMC
  • Authorization number:
  • PL 12064/0002
  • Last update:
  • 22-07-2019

Summary of Product characteristics: dosage, interactions, side effects

Object 1

Bismuth Subnitrate and Iodoform Paste

Impregnated Gauze

Summary of Product Characteristics Updated 18-Feb-2015 | Martindale Pharma

1. Name of the medicinal product

Bismuth Subnitrate and Iodoform Paste Impregnated Gauze.

2. Qualitative and quantitative composition

A lemon yellow paste impregnated gauze with characteristic antiseptic odour.

The gauze is impregnated with a paste of composition.

Bismuth Subnitrate

BPC 1973

20% w/w.

Iodoform

BPC 1954

40% w/w.

Paraffin Liquid

40% w/w.

3. Pharmaceutical form

A paste impregnated gauze.

4. Clinical particulars

4.1 Therapeutic indications

a) Post ENT Surgical Procedures

As an antiseptic gauze used to prevent infection and thus assist healing following ENT procedures.

It is not recommended that the impregnated gauze be placed into open wounds.

b) Acute Epistaxis

To pack the nasal cavity in order to reduce/stop the flow of blood.

4.2 Posology and method of administration

a) In ENT surgical procedures

Sufficient impregnated gauzes should be packed into the cavity to protect the operation site from bacterial

challenge. The gauze is left in place until the wound has healed or graft taken.

It is not recommended that the impregnated gauze be placed into open wounds.

b) Acute epistaxis

Sufficient impregnated gauze(s) is packed up in the nose to stop the blood flow. The gauze is removed the

following day or when clinical judgement dictates.

4.3 Contraindications

Known hypersensitivity to Iodoform, iodine and bismuth.

4.4 Special warnings and precautions for use

Use with caution with patients suffering from hyperthyroidism.

4.5 Interaction with other medicinal products and other forms of interaction

None known.

4.6 Pregnancy and lactation

There is insufficient evidence of safety in pregnancy, as with all drugs it is not recommended the product

is used in pregnancy.

4.7 Effects on ability to drive and use machines

Not applicable.

4.8 Undesirable effects

Hypersensitivity to iodine can result in an erythematous rash, which subsides on removal of the gauze.

Although rare, there are reports within the published literature of the development of encephalopathy

associated with the application of BIPP, however none of the cases reported have occurred following

ENT procedures.

4.9 Overdose

Severe iodine poisoning is characterised by headache, somnolence, delirium and rapid feeble pulses.

General supportive procedures are required. Overdose is not usually a problem when gauzes are packed in

small cavities associated with the middle ear and mastoid operations.

5. Pharmacological properties

5.1 Pharmacodynamic properties

Iodoform:-

Has a marked anaesthetic and antiseptic action due to the release of iodine.

Bismuth subnitrate:-

Bismuth subnitrate action is both as an astringent and absorbent.

5.2 Pharmacokinetic properties

Pharmacokinetic particulars are not applicable since the active constituents are not systemically absorbed.

5.3 Preclinical safety data

Not applicable

6. Pharmaceutical particulars

6.1 List of excipients

Paraffin Liquid BP

X-Ray detectable Fast Edge Ribbon Gauze

May also contain Purified water BP.

6.2 Incompatibilities

The paste is incompatible with oxidising agents - lead, silver and mercuric salt.

6.3 Shelf life

2 years

6.4 Special precautions for storage

Store between 2-8°C. Protect from light.

6.5 Nature and contents of container

An Aluminium laminated pouch of composition:

Polyester

12 micron

Polythene

20g/m2

Aluminium

9 micron

Surlyn

50g/m2

6.6 Special precautions for disposal and other handling

Discard any unused gauze at the end of a procedure or session. Do not use if the pouch is damaged.

7. Marketing authorisation holder

Aurum Pharmaceuticals Limited

Bampton Road

Harold Hill Romford

Essex RM3 8UG

8. Marketing authorisation number(s)

PL 12064/0002

9. Date of first authorisation/renewal of the authorisation

12th January 1995

10. Date of revision of the text

June 2002

Company Contact Details

Martindale Pharma

Address

Bampton Road, Harold Hill, Romford, Essex, RM3 8UG

Telephone

+44 (0)1277 266 600

Medical Information e-mail

[email

protected]

http://www.martindalepharma.co.uk

+44 (0)1277 848 976

Customer Care direct line

+(0)800 137 627