Dna Liquid
FDA Label NDC 52654-0002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Chi Research Inc for the product Dna (NDC 52654-0002). 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, directions, inactive ingredients, keep out of reach of children, indications and usage, questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

DNA 12X

Indications

For temporary relief of symptoms associated with cellular detox.

Warnings

If pregnant or breast feeding, ask a health professional before use. Consult a physician for use in children under 12 years of age.

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.

Directions

Adults and children 5 drops twice daily or as otherwise directed. If symptoms persist, consult your health care professional.

Inactive Ingredients

Demineralized water, 20% Ethanol.

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.

Indications And Usage

For temporary relief of symptoms associated with cellular detox.

Questions

Distributed by

Chi Research, Inc.

207 6th Street South

Walker, MN 56484

218-547-1775

Package Label.Principal Display Panel

CHI

RESEARCH

DNA 12X

Homeopathic Remedy

2 fl. oz. (60 ml)

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