Plus Relief Gel
FDA Label NDC 47219-312

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Nutra Pharma Corporation for the product Plus Relief (NDC 47219-312). 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 active ingredients, purpose, directions:, indications & usage, inactive ingredients:, warnings:, pregnancy, otc - do not use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Active Ingredients

→ Purpose

→ Directions:

→ Indications & Usage

→ Inactive Ingredients:

→ Warnings:

→ Pregnancy

→ Otc - Do Not Use

→ Principal Display Panel - 2 Oz Bottle Label

Active Ingredients

Asian Cobra Venom 6X

Purpose

Analgesic*

*Claims based on traditional Homeopathic practice not accepted medical evidence. Not FDA accepted.

Directions:

Remove protective wrapping.
Liberally apply gel to affected area.
Rub thoroughly into hands and joints.

Indications & Usage

USE 3-4 TIMES A DAY.

Note:It may take several days to induce relief. Use within 90 days of opening. Store at 50° to 80°F.

Inactive Ingredients:

Benzalkonium Chloride, Ethanol, Methocel, Propylene glycol, Saline.

NDC 47219-312-02■ HOMEOPATHIC

Warnings:

For external use only.
If pain persists, consult a physician.
Avoid contact with eyes. If product gets into eyes, flush with water. Seek medical attention.
Not for use on open wounds.