Prebiotic + Probiotic With Colostrume Lactobacillus Acidophilus 250 million + Lactobacillus Rhamnosus 250 Million + Lactobacillus Paracasei 250 million + Bifidobacteruim Longum 200 million + Bifidobacterium Bifidum 200 million + Saccharomyees Boulardii 10

Prebiotic + Probiotic With Colostrume Lactobacillus Acidophilus 250 million + Lactobacillus Rhamnosus 250 Million + Lactobacillus Paracasei 250 million + Bifidobacteruim Longum 200 million + Bifidobacterium Bifidum 200 million + Saccharomyees Boulardii 100 million + Streptoeoeeus Thermophilus 150 million + Fructo Oligo Saccharides 100 mg + Colostrums 100 mg (Hard Gelatin Cap) is a hard gelatin capsule formulated with Prebiotic + Probiotic With Colostrume Lactobacillus Acidophilus 250 million + Lactobacillus Rhamnosus 250 Million + Lactobacillus Paracasei 250 million + Bifidobacteruim Longum 200 million + Bifidobacterium Bifidum 200 million + Saccharomyees Boulardii 100 million + Streptoeoeeus Thermophilus 150 million + Fructo Oligo Saccharides 100 mg + Colostrums 100 mg ( Cap). The listed active ingredient profile is Prebiotic; Probiotic With Colostrume Lactobacillus Acidophilus; Lactobacillus Rhamnosus; Lactobacillus Paracasei; Bifidobacteruim Longum; Bifidobacterium Bifidum; Saccharomyees Boulardii; Streptoeoeeus Thermophilus; Fructo Oligo Saccharides; Colostrums, placing the product in the probiotic / gastrointestinal support category. The formulation provides selected probiotic organisms and/or supportive nutritional components for gastrointestinal microbial support. The source identifies the dosage form as hard gelatin 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.