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STOCCEL -P (Oral suspension)

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  • 20 
  • Vietnam
  • Ho Chi Minh City
  • Two years
  • Aluminium phosphate gel 20%
  • Treatment of acute,chronic gastritis gastro-duodenal ulcer hiatal oesophageal hernia gastroesophageal refux
Post Date : August 18
Product Details
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Item specifics

Vietnam
Ho Chi Minh City
Two years
Aluminium phosphate gel 20%
4SCK01
Gastrointestinal Agents
Powder
Sunnet
L/C,T/T
DHG PHARMA
Antacid
40,000 Box/Boxes per Month

Specifications

Treatment of acute and chronic gastritis, gastro-duodenal ulcer, hiatal oesophageal hernia, gastro esophageal refux.

DESCRIPTION
Antacids, treatment of duodenal ulcer

COMPOSITION
Aluminium phosphate gel 20%... 12.38 g
Excipients q.s.................................... 1 sachet
(Mannitol, pectin, refined sugar, sunett sugar, orange essential oil, sodium hydroxide, sodium benzoate, potassium sorbate, purified water).
DOSAGE FORM
Oral suspension.
PRESENTATION
Box of 25 sachets x 20 g of oral suspension.
ACTIONS
Stoccel P containing aluminium phosphate is used as a gastric antacid in the form of gel. Aluminium phosphate decreases excessive gastric acid but does not cause neutralization: the collodial gel contained in Stoccel P provides a mucus-like protective film which covers a large section of the digestive tract mucosa. The protective film containing the finely dispersed aluminium phosphate allows rapid healing of inflammation and ulceration, protects the gastric mucosa from external influences, and thus rapidly alleviates the patient's discomfort. Stoccel P is not normally absorbed and affected the acid-alkaline balance of the body. Aluminium phosphate slowly dissolves in the stomach and reacts with hydrochloride acid to form aluminium chloride and water. The formed aluminium chloride is absorbed and excreted via the kidney; the unabsorbed aluminium phosphate will be expelled via the stools. Aluminium phosphate has a strong point of not affecting the phosphate absorption in the gastrointestinal tract.
INDICATIONS
Treatment of acute and chronic gastritis, gastro-duodenal ulcer, hiatal oesophageal hernia, gastro esophageal refux, and complications (oesophagitis), heartburn and indigestion. Treatment of toxicosis of acid, alkaline or corrosives causing haemorrhage.
CONTRAINDICATIONS
No documents have been reported.
PRECAUTIONS
Chronic severe renal impairment.
INTERACTIONS
Stoccel P diminishes the absorption of iron salt, cycline, fluoroquinolone, anti-tuberculosis drugs, anti-histamine H2, sodium fluoride in case of concomitant administration by oral route; therefore, the oral interval between of Stoccel P and above substances should be over 2 hours.
ADVERSE EFFECTS
Constipation, particularly in the elderly; so taking much water is recommended to these patients.
Inform your physician about any adverse effects occur during the treatment.
DOSAGE & ADMINISTRATION
Adults: oral dose of 1 - 2 sachets x 2 - 3 times daily.
It is advisable to take the drug at the interval between 2 meals (1-3 hours after main meals)
The oral interval between Stoccel P and other drugs should be 2 hours.
Or as directed by the physician.
Read the directions carefully before use.
Consult the physician for more information.
SHELF-LIFE
24 months from the manufacturing date.
STORAGE CONDITIONS
Store in cool, dry places; protected from light.
SPECIFICATIONS
Manufacturer's.

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SORBITOL (Powder)

SORBITOL (Powder)

SORBITOL (Powder)

Symptomatic treatment of constipation, gastrointestinal disturbances, choleretic.

DESCRIPTION
Treatment of constipation, digestive disorders, biligenic

COMPOSITION
Sorbitol ........................ 5 g
DOSAGE FORM
Powder.
PRESENTATION
Box of 20 sachets x 5 g powder.
ACTIONS
Sorbitol promotes the hydration of intra-intestinal substances. Sorbitol stimulates the secretion of cholecystokinin - pancreazymine, accelerates intestinal peristalsis, fluidifies the stools by its osmotic effect.
INDICATIONS
Symptomatic treatment of constipation, gastrointestinal disturbances, choleretic.
CONTRAINDICATIONS
Biliary tract obstruction.
Abdominal pain of unknown origin.
PRECAUTIONS
Prolonged use of laxatives is not recommended. Treatment of constipation with sorbitol is o­nly an adjunct to hygienic-dietetic treatment. In patients with colophathy, avoid administration of sorbitol while hunger and reduce the dosage.
INTERACTIONS
Avoid concomitant administration with kayexalate (by oral administration or putting in anus) because of the risk of colon necrosis.
ADVERSE EFFECTS
Possibility of diarrhoea, abdominal pains, especially in patients with functional colophathy. Inform your physician about any adverse effects occur during the treatment.
DOSAGE & ADMINISTRATION
Dissolve the powder in some fresh water.
* Gastrointestinal disturbances: Take the drug before meals or when symptoms occur.
Adults: oral dose of 1 - 3 sachets daily.
Children: half the dose of the adults.
* Constipation: Take the drug at early morning or before bedtime.
Adults: oral dose of 1 - 2 sachets.
Children: half the dose of the adults.
Or as directed by the physician.
Read the directions carefully before use.
Consult the physician for more information.
SHELF-LIFE
24 months from the manufacturing date.
STORAGE CONDITIONS
Store in cool, dry places; protected from light.
SPECIFICATIONS
Manufacturer's.
(The active ingredient - Sorbitol is manufactured in France).
Detail more >>
KIM TIEN THAO - RAU MEO (Medicine)

KIM TIEN THAO - RAU MEO (Medicine)

KIM TIEN THAO - RAU MEO (Medicine)

Treatment of urolith: nephrolith, cystolith, ureterolith, cholelith.
Supportive therapy for pyelitis, cholecystitis,hepatitis.

DESCRIPTION
Treatment of Nephrolith

COMPOSITION:

Ext. Desmodium styracifolium …….. 200 mg

Ext. Orthosiphon stamineus ……….… 100 mg

Excipients q.s ..................................... 1 tablet

(Wheat starch, avicel, aerosil, magnesium stearate, sugar, talc, gum arabic, titanium dioxide, HPMC, PEG 6000, nipagin M, PVA, red ferric oxide, black ferric oxide, carnauba wax, hard paraffin).

DOSAGE FORM:

Sugar coated tablets.

PRESENTATION:

Box of 100 sugar coated tablets.

ACTIONS:

Kim tien thao Rau meo is a combination of natural medicinal herbs such as Desmodium styracifolium and Orthosiphon stamineus which have effects o­n treatment of urinary tract diseases.

Desmodium styracifolium (Osb) belongs to the Fabaceae family.

According to popular experiences, Desmodium styracifolium has been used to treat gall-bladder calculus, renal calculus, vesical calculus, oedema, nephritides, and indigestion.

According to modern medicine researches, Desmodium styracifolium has effects o­n diuretic, choleretic, anti-inflammation, vasodilation, hypotension. By the diuretic effect, the minor-molecules such as calcium oxalate and calcium phosphate are drifted down the urine flow; this reduces condensation and prevents an increase in size of stones formed in renal tubular. Besides, Desmodium styracifolium, by the anti-inflammatory property, reduces urinary tract infections and inflammations, ureteral oedema; creates good conditions to push stones out, and relieves the symptoms of urodynia or frequent urination, oedema.

According to the clinical research results, Desmodium styracifolium is effective in the treatment of calcium oxalate stones. The therapy period depends o­n stone’s size and position in the urinary tract.

Orthosiphon stamineusBenth belongs to Lamiaceae family.

According to the popular experiences, Orthosiphon stamineus has been used as a diuretic in treatment of renal calculus, gall-bladder calculus.

According to the pharma-clinical researches, Orthosiphon stamineus is very helpful in treatment of renopathy and oedema. Orthosiphon stamineus contains orthosiphonin and potassium salts which have effects o­n keeping uric acid, urate salts in dissolving form and increasing the excretion of citrate and oxalate into the urine. Consequently, Orthosiphon stamineus helps to prevent the deposition of citrate, oxalate in the body and obstruct the formation of renal calculus.

INDICATIONS:

Treatment of urolith: nephrolith, cystolith, ureterolith, and cholelith.

Supportive therapy for pyelitis, cholecystitis, hepatitis, jaundice.

For the treatment of oedema, urodynia, and frequent urination.

CONTRAINDICATIONS:

Hypersensitivity to any components of the drug.

PRECAUTIONS:

The product should not be administered to pregnant women.

Patients with stomachache should take the drug in a full stomach.

INTERACTIONS:

No cases have been reported.

ADVERSE EFFECTS:

No cases have been reported.

Inform your physician about any adverse effects occur during the treatment.

OVERDOSAGE:

No document has been reported.

DOSAGE & ADMINISTRATION:

Adults: oral dose of 3 - 4 tablets x 3 times daily, with a lot of fresh water.

Or as directed by the physician.

Read the directions carefully before use.

Consult the physician for more information.

Shelf-life: 24 months from the manufacturing date.

Storage conditions: Store in cool, dry places; protect from light.

Specifications: Manufacturer's

Detail more >>
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