Source of supply
Fields of Application
Wound treatment
Antiseptic treatment of traumatic, acute, chronic, surgical and burn wounds.Mucous membrane antiseptic
- prior to diagnostic and surgical interventions in the anogenital (e.g. before obliteration of haemorrids), the urogenital area (e.g. before placing an intra-uterine device (IUD), the vaginal area, before prenatal, intranatal and postnatal manipulations) and in the oral cavity (e.g. before tooth extractions)
- before placing urinary tract catheters
- for preop. skin antisepsis in the area close to mucous membranes
Instructions for use
- Moisturize the treated area evenly and thoroughly with the antiseptic.
- Swab method: Rub concerned areas with saturated swabs. Swabbing is the prefered method of application.
- Spray method: In individual cases spray octenisept® directly on poorly accessible areas of the skin and mucous membrane. Make sure all areas are evenly moistened.
- octenisept® may also be applied by rinsing the oral cavity
Product data
Composition:
100g solution contains: Octenidine dihydrochloride 0.1g, 2-Phenoxyethanol (Ph.Eur.) 2.0g
Other ingredients:
cocamidopropylbetaine, sodium D gluconate, glycerol 85%, sodium chloride, sodium hydroxide, purified water
Special advice
- To prevent possible tissue injury, the product must not be injected into the deep tissue using a syringe. The product is intended for superficial use only (application by swab or spray pump).
- octenisept® should not be used for irrigating the abdominal cavity (e.g. intraoperatively), the urinary bladder and nose or eardrum.
- Do not swallow octenisept®.
- Do not enter it into the blood circuit, e.g. by being accidently injected.
- Do not mix octenisept® with other compounds.
- Do not use octenisept® in combination with PVP-iodine based antiseptics.
- Bandages and incision foils can be applied after octenisept® has dried off completely.
- In rare cases octenisept® may cause slight burning.
- octenisept® can be heated up to body temperature.
- octenisept® expires three years after opening.
- Once the container has been opened octenisept® should not be used for more than three years but not beyond the expiry date.
- As a general prinicple: administrating of any pharmaceuticals within the first trimester of pregnancy should be carried out under strict indication and medical supervision.
- Microbiological efficacies on specific germs have only been carried out in in-vitro tests.
- Usage of octenisept® in the eye should be avoided. In case of contact with eyes, rinse immediately with plenty of water.
- Do not freeze.
Information for order
| Item | Delivery form | Item | GTIN |
|---|---|---|---|
| octenisept KP 500 ml FL | 20 / carton(s) | 173706 | 4032651737062 |
| octenisept mit Sprühpumpe 250 ml FL | 10 / carton(s) | 121411 | 4032651214112 |
| octenisept KP 1 l FL | 10 / carton(s) | 173704 | 4032651737048 |
| octenisept 250 ml FL | 10 / carton(s) | 121406 | 4032651214068 |
| octenisept 1 l FL | 10 / carton(s) | 121403 | 4032651214037 |
| octenisept colourless -CH- 50 ml FL | 20 / carton(s) | 121460 | 7680498531496 |
| octenisept KP 250 ml FL | 10 / carton(s) | 173702 | 4032651737024 |
| octenisept 500 ml FL | 20 / carton(s) | 121464 | 4032651214648 |
| octenisept KP mit Sprühpumpe 250 ml FL | 10 / carton(s) | 173711 | 4032651737116 |
Application aids
| Item | Delivery form |
|---|---|
| Spray pump CE standard DIN 32 500/1000ml | 10 / carton(s) |
| wall bracket plastics 500ml | 1 |
Accessories
| Item | Delivery form |
|---|---|
| wall bracket plastics 500ml | 1 |
Related products
octenisept®
Active substances: octenidine dihydrochloride, phenoxyethanol (Ph.Eur.). Composition: 100 g solution contain: 0.1 g octenidine dihydrochloride, 2.0 g phenoxyethanol (Ph.Eur.). Other ingredients: cocamidopropylbetaine, sodium D gluconate, glycerol 85%, sodium chloride, sodium hydroxide, purified water. Indications: For repeated, short-term antiseptic treatment of mucous membranes and adjacent tissues prior to diagnostic and surgical procedures - in the ano-genital region including the vagina, vulva and glans penis as well as prior to bladder catheterization - in the oral cavity. For short-term supporting therapy of interdigital mycotic infections and adjuvant antiseptic wound treatment. Contraindications: octenisept® may not be used in cases of hypersensitivity to any of the components of the preparation. octenisept® should not be used for rinsing the abdominal cavity (e.g. intra-operatively) or the bladder, nor the tympanic membrane. Undesirable effects: rare: burning, redness, itching and warmth at the application site, very rare: allergic contact reaction, e.g. temporary redness at the application site; frequency unknown: after lavage of deep wounds with a syringe, persistent edema, erythema and also tissue necrosis have been reported, in some cases requiring surgical revision. Rinsing of the oral cavity may cause a transitory bitter sensation. Revision 11/22
To prevent possible tissue injury, the product must not be injected into the deep tissue using a syringe. The product is intended for superficial use only (application by swab or spray pump).
Schülke & Mayr GmbH, 22840 Norderstedt, Germany, Tel. +49 40 52100-666, info@schuelke.com
More information
*Please read the package leaflet.