Source: Medicines & Healthcare Products Regulatory Agency (GB) Revision Year: 2022 Publisher: Neon Healthcare Ltd., 8 The Chase, John Tate Road, Hertford, SG13 7NN, United Kingdom
Zineryt 40 mg + 12 mg powder and solvent for cutaneous solution.
| Pharmaceutical Form |
|---|
|
Powder and solvent for cutaneous solution. The packaging contains a bottle of powder, a bottle of solvent and an applicator in a plastic holder. |
Erythromycin-zinc complex containing the equivalent of 40 mg/ml erythromycin and 12 mg/ml zinc acetate dihydrate (as the complex) on constitution.
For the full list of excipients, see section 6.1.
| Active Ingredient | Description | |
|---|---|---|
| Erythromycin |
Erythromycin exerts its antimicrobial action by binding to the 50S ribosomal sub-unit of susceptible microorganisms and suppresses protein synthesis. Erythromycin is bacteriostatic and bactericidal depending on its concentration and the type of organism. |
|
| Zinc acetate |
The active moiety in zinc acetate is zinc cation, which blocks the intestinal absorption of copper from the diet and the reabsorption of endogenously secreted copper. |
| List of Excipients |
|---|
|
Diisopropyl sebacate |
Screw-capped HDPE bottles; an applicator assembly is fitted when dispensed. When constituted packs are of 30 ml and 90 ml.
Neon Healthcare Ltd., 8 The Chase, John Tate Road, Hertford, SG13 7NN, United Kingdom
PL 45043/0097
Date of first authorisation: 07 March 1990
Date of latest renewal: 19 December 2008
| Drug | Countries | |
|---|---|---|
| ZINERYT | Cyprus, Spain, Ireland, Malta, Poland, Romania, United Kingdom, South Africa |
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