Venodol
FDA Label NDC 71181-100

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Caretta Therapeutics for the product Venodol (NDC 71181-100). 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 otc - purpose, otc - keep out of reach of children, principal display panel - ndc: 71181-100-02 - roll-on bottle label, principal display panel - ndc: 71181-100-02 - roll-on box label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Purpose

Active IngredientPurpose
Cobra Venom (Naja naja) 4x (0.1 mg/gm) HPUS....Analgesic
(Per Homeopathic Pharmacopoeia of the United States)

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children.

Principal Display Panel - Ndc: 71181-100-02 - Roll-On Bottle Label

Roll-on Bottle Label (Venodol Roll On 01)

Roll-on Bottle Label (Venodol Roll On 01)



Principal Display Panel - Ndc: 71181-100-02 - Roll-On Box Label

Roll-on Box Label (Venodol Roll On 02)

Roll-on Box Label (Venodol Roll On 02)



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