Bio-scriptives Extreme Pr
FDA Label NDC 60608-015

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Biochemics, Inc. for the product Bio-scriptives Extreme Pr (NDC 60608-015). 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 ingredient, purpose, uses, warnings, stop use and ask doctor if, otc - keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Natural Menthol 4.4%

Purpose

Analgesic

Uses

For temporary relief of minor aches and pains of muscles and joints associated with arthritis, sprains, strains, and back pain.

Warnings

■  Avoid Contact with eyes.■  Do not use on wounds or damaged skin.For external use only.

Stop Use And Ask Doctor If

■  condition worsens/lasts more than 7 days.

Otc - Keep Out Of Reach Of Children

Keep out of the reach of children.

Directions

■  Do not use if safety seal is broken.
■  Shake well before each application.
■  Apply and massage Extreme PR™ onto treatment area up to 4 times daily.


Inactive Ingredients

Deionized Water, Isopropanol, Olive Oil, Propylene Glycol, Eucalyptus Oil, Sodium Alginate, Cetyl Alcohol, Glyceryl Stearate and PEG-100 Stearate, Kelp Extract, Marshmallow Extract, Allantoin, and Xanthan Gum.

Questions:

Distributed by BioChemics

dba Bio-Scriptives (978) 750-0790

99 Rosewood Drive, #260

Danvers, MA 01923


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