Cactus
FDA Label NDC 60986-1028

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Marco Pharma International Llc. for the product Cactus (NDC 60986-1028). 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, otc - keep out of reach of children, dosage, warnings, dosage & administration, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

Midland Hathorne 1XHPUS

Night Blooming Cerus 2XHPUS

Lily of the Valley 3XHPUS

Natural Camphor 2XHPUS

Mountain laurel 4XHPUS

Pinkroot 4XHPUS

Bushmaster viper 8XHPUS

Mountain Arnica 6XHPUS

Tabacco 8XHPUS

Nitroglycerin 8XHPUS

The letters HPUS indicates that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of United Sates.

Purpose

FOR RELIEF OF CHEST PAIN DUE TO STRESS; ANGINA PECTORIS; MYOCARDIAL INSUFFICIENCY; TOBACCO ABUSE.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Dosage

Adults take 30 drops in 1 oz water three times daily. For acute symptoms, take 40 drops four to five times daily. Children receive 10 drops in 1 oz tepid water three time daily.

Warnings

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

Dosage & Administration

(Read Suggested Use Section)

Package Label.Principal Display Panel

Cactus.jpg

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