Human Formulations

Methylcobalamin 1500mcg + Alpha lipoic Acid 200mg + Benfotiamine 50mg + Bs3mg + Biotin 5mg + Follc Acid 1.5mg

Methylcobalamin 1500mcg + Alpha lipoic Acid 200mg + Benfotiamine 50mg + Bs3mg + Biotin 5mg + Follc Acid 1.5mg is a capsule formulated with Methylcobalamin 1500mcg + Alpha lipoic Acid 200mg + Benfotiamine 50mg + Bs3mg + Biotin 5mg + Follc Acid 1.5mg. The l

CapsulesNon-Beta-Lactam Capsules Single Ingredient Capsule
Sterile injectable formulation

Product information

Product Line
Human Formulations
Category
Capsules, Non-Beta-Lactam Capsules
Dosage Form
Capsule
Product Type
Single Ingredient

Available strengths

Methylcobalamin 1500mcg + Alpha lipoic Acid 200mg + Benfotiamine 50mg + Bs3mg + Biotin 5mg + Follc Acid 1.5mg

Description

Methylcobalamin 1500mcg + Alpha lipoic Acid 200mg + Benfotiamine 50mg + Bs3mg + Biotin 5mg + Follc Acid 1.5mg is a capsule formulated with Methylcobalamin 1500mcg + Alpha lipoic Acid 200mg + Benfotiamine 50mg + Bs3mg + Biotin 5mg + Follc Acid 1.5mg. The listed active ingredient profile is Methylcobalamin; Alpha lipoic Acid; Benfotiamine; Bs3mg; Biotin; Follc Acid, placing the product in the neuropathic pain / neuro-nutritional category. The formulation contains neuropathic-pain and/or neuro-nutritional components used in selected nerve-related conditions under clinician guidance. The source identifies the dosage form as capsule with not specified presentation. For website cataloguing, the composition, strength, dosage form and formulation characteristics should be displayed prominently and consistently. The product description should remain factual and should not include unapproved cure, superiority, guaranteed-result or broad therapeutic claims. Clinical selection should depend on diagnosis, patient-specific factors, contraindications, concomitant medicines and professional judgement. Prescription status, warnings, interactions, adverse effects and dosing or application instructions must be checked against the current approved product label. Manufacturer, licence, storage, shelf-life, reconstitution where applicable, and market-specific regulatory details should be added only from verified product documentation.
WHO-GMP Sourced
Sterile Supply
Regulatory Documentation
Quality Assured