Am-13 Solution
FDA Label NDC 58264-0352

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Dna Labs, Inc. for the product Am-13 (NDC 58264-0352). 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 other, otc - purpose, ingredients, suggested dosage, storage and handling, otc - pregnancy or breast feeding, otc - keep out of reach of children, principal display panel - 1 fl. oz. bottle label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Other

→ Otc - Purpose

→ Ingredients

→ Suggested Dosage

→ Storage And Handling

→ Otc - Pregnancy Or Breast Feeding

→ Otc - Keep Out Of Reach Of Children

→ Principal Display Panel - 1 Fl. Oz. Bottle Label

Other

NDC 58264-0352-1

Use only if cap seal is unbroken.

To be used according to standard homeopathic indications.

Otc - Purpose

Regulates energy flow to the governor vessel meridian.

Ingredients

Argentum nitricum 6x, Carboneum sulphuratum 30x, Corallium rubrum 30x, Cuprum arsenicosum 8x, Ginseng 3x, Hypericum perforatum 6x, Lathyrus sativus 30x, Acidum picricum 12x, Selenium metallicum 30x, Stramonium 30x, Zincum metallicum 30x, aa partes, 20% alcohol in purified water.