Nimulide gel for external use, 1%, 30 g

Special Price $13.58 Regular Price $22.00
In stock
SKU
OTC10203043
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Category

Anesthesia and muscle relaxants

,

Bruises, sprains

Scope of the drug

Musculoskeletal system

Release form

Gel

Manufacturer country

India

Package quantity, pcs

one

Description

Nimulide gel d / nar.

approx.

1% tube 30g

Name ENG

NIMULID

Clinical and pharmacological group

NSAIDs for external use

ATX code

Non-steroidal anti-inflammatory drugs for external use

Dosage

1% x 30g

Structure

Active ingredient: nimesulide 10 mg

Excipients: hyprolosis

carbomer

ethyl alcohol 95% (purified)

purified water

triacetin

dimethylacetamide

phosphoric acid

flavoring MSC-03

flavor 0106-G

Storage conditions and periods

In a place protected from direct sunlight, at a temperature not exceeding 25 degrees, in a sealed package (away from fire, do not store in a refrigerator).

Expiration date: 3 years

INN / Active ingredient

Nimesulide

Specifications

Category

Anesthesia and muscle relaxants

,

Bruises, sprains

Scope of the drug

Musculoskeletal system

Release form

Gel

Manufacturer country

India

Package quantity, pcs

one

Way of introduction

Outwardly

Vacation conditions

Without recipe

Brand name

Panacea Biotec

The amount of the dosage form in the primary package

30 g

Primary packaging type

Plastic tube

Type of consumer packaging

Pack of cardboard

Pharmaco-therapeutic group

NSAIDs

Anatomical and therapeutic characteristics

M01AX17 Nimesulide

Dosage form

Gel for external use

Packaging

Box

Drug action

Anti-inflammatory

,

Analgesic

,

Antipyretic

The target audience

Adult

Dosage (volume) of the substance in the preparation

Gel for external use 1% 1 g, nimesulide 10 mg

Expiration date in days

1095

Package weight, g

45

Mode of application

:

For external use.

The areas of the skin treated with the gel should not be covered with occlusive dressings.

The gel should also not be strongly rubbed into the skin.

Apply approximately 3 cm of gel 3-4 times a day to the affected area.

The dose, however, may vary depending on the size of the treated area and the patient's response.

The result of therapy is assessed after 4 weeks.

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