octenisept®

水性創傷・粘膜消毒剤
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  • broad spectrum of antiseptic efficacy
  • fast onset of action
  • very good skin and mucous membrane tolerance
  • suitable for infants and premature babies*
  • safe use during pregnancy (after the first trimester)¹
  • painless and colourless treatment

Source of supply

 

Further information

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

Microbiological efficacy

Recommended use concentration*
Test method
* including phase 2 step 1 as well as phase 2 step 2 tests

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

ItemDelivery formItemGTIN
octenisept KP 1 l FL10 / carton(s)1737044032651737048
octenisept 1 l FL10 / carton(s)1214034032651214037
octenisept 500 ml FL20 / carton(s)1214644032651214648
octenisept 250 ml FL10 / carton(s)1214064032651214068
octenisept mit Sprühpumpe 250 ml FL10 / carton(s)1214114032651214112
octenisept KP 250 ml FL10 / carton(s)1737024032651737024
octenisept KP mit Sprühpumpe 250 ml FL10 / carton(s)1737114032651737116
octenisept KP 500 ml FL20 / carton(s)1737064032651737062

Application aids

ItemDelivery form
Spray pump CE standard DIN 32 500/1000ml
10 / carton(s)
wall bracket plastics 1l
1
wall bracket plastics 500ml
1

Environmental information

schülke manufactures products economically and with advanced, safe and environmentally friendly production processes while at the same time maintaining out high quality standards.

¹Briese et al. (2010): Efficacy and tolerability of a local acting antiseptic agent in the treatment of vaginal dysbiosi during pregnancy; in Arch Gynecol Obste
*Please read the package leaflet.

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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

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