Biovem
FDA Label NDC 69883-001

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Biovem for the product Biovem (NDC 69883-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding warnings, directions for use, otc - keep out of reach of children, otc - active ingredient, inactive ingredient, otc - purpose, otc - pregnancy or breast feeding, uses, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Warnings

For oral use only

If symptoms persist stop using this product and consult a physician

Side effects may include headache, nausea, sore throat

Directions For Use

Dissolve one (1) strip under the tongue daily. It may take up to 15 doses to start relief.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Otc - Active Ingredient

Naja Naja H 10X

Inactive Ingredient

Carboxymethyelcellulose, sodium chloride 0.9%, water, natural orange flavorings, sucrose , thimerosol

Otc - Purpose

Immune Modulator

Otc - Pregnancy Or Breast Feeding

Not for use by pregnant or nursing women

Uses

Temporarily reduces joint inflammation and pain and general associated pain.

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