Enviroforce Liquid
FDA Label NDC 43857-0630

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Bioactive Nutritional, Inc. for the product Enviroforce (NDC 43857-0630). 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:, warnings:, keep out of reach of children:, directions:, indications:, inactive ingredients:, questions:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients:

Sarsaparilla 3X, Xanthoxylum Fraxineum 3X, Phytolacca Decandra 4X, Hydrastis Canadensis 5X, Aurum Metallicum 12X, Carbo Animalis 12X, Causticum 12X, Iodium 12X, Sulphur 30X, Thuja Occidentalis 30X.

Purpose:

For temporary relief of minor pains, skin irritations, & minor swellings in joints with heat.

Warnings:

If pregnant or breast-feeding, ask a health care professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if tamper evident seal is broken or missing.

Store in a cool, dry place.

Keep Out Of Reach Of Children:

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions:

10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

Indications:

For temporary relief of minor pains, skin irritations, & minor swellings in joints with heat.

Inactive Ingredients:

Demineralized Water, 25% Ethanol

Questions:

Distributed by:

BioActive Nutritional, Inc.

1803 N. Wickham Rd.

Melbourne, FL 32935

bioactivenutritional.com

Package Label Display:

BioActive Nutritional

ENVIROFORCE

HOMEOPATHIC

1 FL OZ (30 ml)

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