Boilx Spray
FDA Label NDC 43695-0012

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Global Naturals, Inc. for the product Boilx (NDC 43695-0012). 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:

Anthracinum 30X, Baptisia Tinctoria 3X, Calcarea Picrata 10X, Echinacea (Angustifolia) 3X, Hepar Sulphuris Calcareum 200C, Mercurius Corrosivus 200C, Pyrogenium 200C.

Indications:

Relieves symptoms associated with Boils.

Relieves symptoms associated with Boils.

Warnings:

If you are pregnant or breast-feeding, seek the advice of a doctor 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 around neck of bottle is missing or broken.

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:

Adults and children over 12, spray twice under the tongue three times per day. For children under 12, consult a doctor prior to use.

Inactive Ingredients:

Alcohol 20% v/v, Purified water.

Questions:

Distributed By: Global Naturals Inc.
PO Box 7574 Milton Keynes, MK119GQ, United Kingdom
1-800-756-4120 Mon/Fri 9AM to 5PM PST

Package Label Display:

BoilX

Boils Relief

HOMEOPATHIC

1.0 FL oz. (30 ml)

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