Composition, form of production and packaging
? Cream for external use from white to white with a yellowish hue, uniform, soft, matte, with a weak characteristic odor.
1 g
dexpanthenol 50 mg
chlorhexidine hydrochloride 5 mg
Auxiliary substances: pantolactone - 5 mg, cetyl alcohol - 36 mg, stearyl alcohol - 24 mg, lanolin - 30 mg, paraffin white soft 100 mg, paraffin liquid 100 mg, macrogol stearate 30 mg, purified water up to 1 g .
3.5 g - aluminum tubes with a polyethylene spout (1) - cardboard packs.
30 g - aluminum tubes with a polyethylene spout (1) - cardboard packs.
100 g - aluminum tubes with a polyethylene spout (1) - cardboard packs.
INSTRUCTION FOR THE SPECIALIST.
Description of the drug approved by the manufacturer for the printed edition of 2016.
PHARMACHOLOGIC EFFECT
The drug with antimicrobial, anti-inflammatory and tissue regeneration-improving action for external use.
Chlorhexidine is an antiseptic that is active against bacteria normally found on the skin or on the skin as a result of wound contamination.
Dexpanthenol in skin cells quickly turns into pantothenic acid, which plays an important role both in the formation and healing of damaged skin.
The drug reduces pain due to the cooling effect. When applied to the surface of the wound, it protects against infection, promoting healing.
Easy to apply and wash off. The cream is lean and does not stick.
PHARMACOKINETICS
Data on the pharmacokinetics of the preparation Bepanten В® plus are not available.
INDICATIONS
- small wounds with the threat of infection (abrasions, scratches, small cuts and scratches, cracks, light burns);
- infected superficial skin lesions;
- cracks in the nipples during breastfeeding;
- chronic wounds (for example, trophic ulcers of the lower leg, decubitus);
- surgical wounds.
DOSING MODE
The cream is applied a thin layer 1 or several times / day on a previously cleaned wound surface or on inflamed skin areas. Treatment of wounds can be carried out both in the open way and with the use of dressings.
SIDE EFFECT
Allergic reactions: hives, itching are possible.
CONTRAINDICATIONS
- for treating or treating the auricle;
- in case of severe, deep and heavily soiled wounds (such injuries require medical intervention);
- Hypersensitivity to the components of the drug.
PREGNANCY AND LACTATION
The drug can be used during pregnancy and during breastfeeding, but it should be avoided on large surfaces of the skin.
SPECIAL INSTRUCTIONS
Avoid contact with the eyes. Do not take internally.
Large areas, heavily soiled and deep wounds, as well as bitten and punctured wounds require medical intervention (due to the risk of developing tetanus).
If the size of the wound for some time remains invariably large or the wound does not heal within 10-14 days, then a doctor's consultation is necessary. This is also necessary in case the edges of the wound are highly hyperemic, the wound suddenly swells, severe pain or damage occurs accompanied by fever (due to the risk of developing sepsis).
OVERDOSE
Data on the overdose of Bepanten В® plus is not available.
DRUG INTERACTION
As a precautionary measure for possible interactions (antagonism or inactivation), do not use Bepanten В® plus simultaneously with other antiseptics.
TERMS OF RELEASE FROM PHARMACY
The drug is approved for use as a means of OTC.
TERMS AND CONDITIONS OF STORAGE
The drug should be stored out of reach of children, at a temperature of no higher than 25 В° C. Shelf life - 3 years.
