Adrenoplex Liquid
FDA Label NDC 43857-0331

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 Adrenoplex (NDC 43857-0331). 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:, indications:, warnings:, keep out of reach of children, directions:, inactive ingredients, questions:, package label display:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients:

Chelidonium Majus 3X, Echinacea (Angustifolia) 3X, Glandula Suprarenalis Bovine 8X, Spleen (Suis) 8X, Carduus Marianus 12X, Lycopodium Clavatum 12X, Natrum Muriaticum 12X, Phosphoricum Acidum 12X.

Indications:

For temporary relief of nervous exhaustion, fatigue and forgetfulness.

For temporary relief of nervous exhaustion, fatigue and forgetfulness.

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 cool, dry place.

Keep Out Of Reach Of Children

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.

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

ADRENOPLEX

HOMEOPATHIC

1 FL OZ (30 ml)

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