Allernest Liquid
FDA Label NDC 60986-1003

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 Allernest (NDC 60986-1003). 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, suggested use, 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

Formic acid                   12xHPUS

Bushmaster Viper           8xHPUS

Purging luffa          6xHPUS

Kerosene               6xHPUS

Poison Ivy    6xHPUS

Spikenard         4xHPUS

Thryallis        4xHPUS

White cedar       4xHPUS

Stinging nettle               4xHPUS

Balloon vine           3xHPUS

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

Purpose

Relief of mild allergic reactions.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Suggested Use

Adults: in acute disorders, take 10 drops every 15 minutes on the tongue or with water until improvement if felt, then take 10 drops less frequently. To maintain balance, take 15 drops three times daily. Children receive 1/2 of the adult amount.

Warnings

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

Dosage & Administration

(Read Suggested Use Section)

Inactive Ingredients

Ethyl Alcohol (29.1% by vol.) and Water

Package Label.Principal Display Panel

Allernest.jpg

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