D-panthenol-Nizhpharm-plus (Cream) Instructions for Use
Marketing Authorization Holder
Nizhpharm JSC (Russia)
ATC Code
D08AC52 (Chlorhexidine in combination with other drugs)
Active Substances
Dexpanthenol (Rec.INN registered by WHO)
Chlorhexidine (Rec.INN registered by WHO)
Dosage Form
| D-panthenol-Nizhpharm-plus | Cream for external use 52.5 mg+8.02 mg/1 g: tubes 25 g, 30 g or 50 g |
Dosage Form, Packaging, and Composition
Cream for external use white or almost white in color.
| 1 g | |
| Dexpanthenol | 52.5 mg |
| Chlorhexidine bigluconate (in the form of a 20% solution) | 8.02 mg |
Excipients: propylene glycol – 100 mg, macrogol cetostearyl ether (Eumulgin B2) – 16 mg, cetostearyl alcohol (cetyl alcohol not more than 60%, stearyl alcohol not less than 40%) (Lanette O) – 54 mg, liquid paraffin (medical vaseline oil) – 100 mg, vaseline – 100 mg, sodium hydrogen phosphate dodecahydrate – 0.2 mg, potassium dihydrogen phosphate – 7.8 mg, purified water – up to 1 g.
25 g – aluminum tubes (1) – cardboard packs.
30 g – aluminum tubes (1) – cardboard packs.
50 g – aluminum tubes (1) – cardboard packs.
Clinical-Pharmacological Group
A drug improving trophism and tissue regeneration, with antimicrobial activity for external use
Pharmacotherapeutic Group
Tissue repair stimulant
Pharmacological Action
A combined drug that improves trophism and tissue regeneration, with antimicrobial activity for external use.
Dexpanthenol is a B vitamin, which is metabolized in the body to pantothenic acid, a component of coenzyme A involved in acetylation processes, carbohydrate and fat metabolism, and the synthesis of acetylcholine, corticosteroids, and porphyrins.
It stimulates skin regeneration, normalizes cellular metabolism, accelerates mitosis, and increases the strength of collagen fibers. It has regenerating, vitamin, metabolic, and anti-inflammatory effects.
Chlorhexidine is an antimicrobial drug, an antiseptic.
Active against gram-positive and gram-negative bacteria, including Staphylococcus spp., Enterococcus spp., Pseudomonas aeruginosa, Escherichia coli, Streptococcus spp., as well as yeast-like fungi and dermatophytes.
It retains activity in the presence of blood, pus, various secretions, and organic substances.
The Depantol cream protects the wound surface from infections, suppresses the course of the infectious process, and accelerates healing.
Pharmacokinetics
Pharmacokinetic data for the drug are not provided.
Indications
- Wound treatment when there is a risk of infection (including abrasions, cuts, scratches, cracks, excoriations, insect bites, burns, trophic ulcers);
- Postoperative wound treatment;
- Treatment of infected wounds, burns (including sunburns), bedsores, abrasions, cuts, cracks, trophic ulcers, intertrigo;
- Treatment of infected dermatoses (including eczema and atopic dermatitis).
- Diaper dermatitis, scratches with signs of infection in children;
- Cracks and inflammation of the mammary gland nipples with signs of infection in nursing mothers.
ICD codes
| ICD-10 code | Indication |
| L22 | Diaper dermatitis |
| L30.3 | Infectious dermatitis (infectious eczema) |
| L30.4 | Erythematous intertrigo |
| L55 | Sunburn |
| L89 | Decubitus ulcer and pressure area |
| L98.4 | Chronic skin ulcer, not elsewhere classified |
| N64.0 | Fissure and fistula of nipple |
| T14.0 | Superficial injury of unspecified body region (including abrasion, bruise, contusion, hematoma, bite of nonvenomous insect) |
| T30 | Burns and corrosions of unspecified body region |
| T79.3 | Posttraumatic wound infection, not elsewhere classified |
| ICD-11 code | Indication |
| EA40 | Tropical phagedenic ulcer |
| EA88.0Z | Infectious dermatitis, unspecified |
| EF60 | Ischemic ulceration of the skin |
| EH40.10 | Diaper dermatitis |
| EH90.Z | Pressure ulcer of unspecified degree |
| EH92 | Dermatoses provoked by friction or mechanical impact |
| EH92.1 | Blister due to friction |
| EK02.20 | Intertriginous dermatitis due to friction, sweating or contact with body fluids |
| EM0Z | Unspecified skin disorder |
| GB23.1 | Fissure or fistula of nipple |
| ME60.2 | Ulcerative skin lesion of unspecified nature |
| ND56.0 | Superficial injury of unspecified body region |
| NE11 | Burn of unspecified body region |
| NF0A.3 | Posttraumatic wound infection, not elsewhere classified |
Dosage Regimen
| The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen. |
Apply a thin layer of the cream to the affected skin area one to several times daily as indicated by the clinical condition.
For postoperative wounds, burns, and trophic ulcers, apply after standard cleansing and debridement of the wound surface.
For infected dermatoses such as eczema, apply to the inflamed and weeping areas to suppress bacterial growth and promote healing.
In nursing mothers with cracked or inflamed nipples, apply the cream to the nipple surface after each breastfeeding session; cleanse the area prior to the next feeding.
For infants and children with diaper dermatitis or infected scratches, apply to the affected areas after each diaper change or following a gentle cleansing with water.
For sunburns and superficial injuries like abrasions and insect bites, apply gently to cover the entire affected area.
The duration of treatment is determined by the rate of healing and the resolution of infection; discontinue if signs of irritation or hypersensitivity appear.
Adverse Reactions
Possible allergic reactions.
Contraindications
- Hypersensitivity to the components of the drug.
Use in Pregnancy and Lactation
During pregnancy and lactation, the use of the drug on large areas should be avoided.
Pediatric Use
Can be used as indicated.
Special Precautions
Avoid getting the cream into the eyes.
Overdose
Data on drug overdose are not provided.
Drug Interactions
Chlorhexidine is incompatible with soap and other anionic substances.
Storage Conditions
Keep out of reach of children at a temperature not exceeding 25°C (77°F).
Shelf Life
Shelf life – 2 years.
Dispensing Status
The drug is approved for use as an over-the-counter product.
Important Safety Information
This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.
Medical Disclaimer
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