Fire

APIL MEL, BAPTISIA, BARYTA CARB, HAMAMELIS, KALI BROM, KALI PHOS, LACHESIS, LILIUM, PETROLEUM, PHOSPHORICUM AC, SPIGELIA ANTH, SULPHUR, VERATRUM VIR ORAL HUMAN PRESCRIPTION DRUG

Fire is an FDA drug label for the active ingredient APIL MEL, BAPTISIA, BARYTA CARB, HAMAMELIS, KALI BROM, KALI PHOS, LACHESIS, LILIUM, PETROLEUM, PHOSPHORICUM AC, SPIGELIA ANTH, SULPHUR, VERATRUM VIR manufactured by NET Remedies administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20210119.

Generic name
APIL MEL, BAPTISIA, BARYTA CARB, HAMAMELIS, KALI BROM, KALI PHOS, LACHESIS, LILIUM, PETROLEUM, PHOSPHORICUM AC, SPIGELIA ANTH, SULPHUR, VERATRUM VIR
Manufacturer
NET Remedies
Product type
HUMAN PRESCRIPTION DRUG
Route
ORAL
Dosage form
N/A
NDC
61626-0106
Application
N/A
Label effective
20210119

About this product

Fire is an FDA-registered drug product whose active ingredient is APIL MEL, BAPTISIA, BARYTA CARB, HAMAMELIS, KALI BROM, KALI PHOS, LACHESIS, LILIUM, PETROLEUM, PHOSPHORICUM AC, SPIGELIA ANTH, SULPHUR, VERATRUM VIR. It is labelled by NET Remedies taken by oral and marketed as a human prescription drug product. Identifiers on file: NDC 61626-0106, label effective 20210119. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing APIL MEL, BAPTISIA, BARYTA CARB, HAMAMELIS, KALI BROM, KALI PHOS, LACHESIS, LILIUM, PETROLEUM, PHOSPHORICUM AC, SPIGELIA ANTH, SULPHUR, VERATRUM VIR are most often described in connection with: temporary relief, neuro-emotional autonomic, nervous system, non psychiatric, disorders vulnerability, related emotions, minor circulation, irregularities fatigue. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

​ACTIVE INGREDIENTS (HPUS*) ​: Contains equal volumes of each in 12X, 30X, and 100X potencies: Apis mel, Baptisia, Baryta carb, Hamamelis, Kali brom, Kali phos, Lachesis, Lilium, Petroleum, Phosphoricum ac, Spigelia anth, Sulphur, Veratrum vir. (*) The letters "HPUS" indicate that the components in the product are officially monographed in the Homeopathic Pharmacopoeia of the United States. (**) Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Indications & Usage

​INDICATIONS FOR USE: ​For temporary relief of the neuro-emotional (autonomic nervous system - non psychiatric) disorders of vulnerability, lost, and related emotions. Minor circulation irregularities, fatigue. Tongue, perspiration, spine, and upper extremity disorders. Temporary relief of chest congestion and minor pain in reproductive organs.**

Dosage & Administration

​DIRECTIONS: ​Spray 9-12 pumps (approximately 1/2 tsp.) directly in mouth 3 times a day or as directed by a licensed health care practicioner. When appropriate, also spray externally on complaint area 3 times daily.

Warnings

​WARNINGS : ​• ​If symptoms persist or worsen ​, seek advice of licensed health care practicioner. • ​If pregnant or nursing ​, take only advice of licensed health care practitioner. • ​Keep this and all medication out of reach of children. • Keep this and all medication out of reach of children.

Recall and safety notices

4 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

RecallProductFirmClassStatusReported
D-0641-2025 Ultra Violette Mini SPF Mates kit includes: Velvet Screen SPF 50 Blurring Mineral SkinScreen, Zinc Oxide 22.75%, 15 mL, 0.5 fl. oz. per tube, Supreme Sunscreen SPF 50, 15 mL 0.5 fl. oz. per tube, Distributed by: Grace & Fire USA Inc., 251 Little Falls Drive, New Castle Wilmington, Delaware 19808, NDC 84803-110-01 (15 mL Velvet Screen), UPC 9355909005757. GRACE & FIRE PTY LTD Class II Ongoing 20250917
D-0640-2025 Ultra Violette, Velvet Screen SPF 50, Blurring Mineral Skinscreen, Zinc Oxide 22.75%, a) 15 mL, 0.5 fl. oz. per tube, NDC 84803-106-01, UPC 9355909006068, b) 50 mL, 1.7 fl. oz. per tube, NDC 84803-106-02, UPC 9355909005924, Distributed by: Grace & Fire USA Inc., 251 Little Falls Drive, New Castle Wilmington, Delaware 19808. GRACE & FIRE PTY LTD Class II Ongoing 20250917
D-1123-2020 Fire Off, 500mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808 Herbal Doctor Remedies Class II Terminated 20200415
D-0945-2019 NET Remedies #5 Fire Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4205-2 King Bio Inc. Class I Terminated 20190320

Frequently asked questions

What is Fire used for?
​INDICATIONS FOR USE: ​For temporary relief of the neuro-emotional (autonomic nervous system - non psychiatric) disorders of vulnerability, lost, and related emotions. Minor circulation irregularities, fatigue. Tongue, perspiration, spine, and upper extremity disorders. Temporary relief of chest congestion and minor pain in reproductive organs.**

Who makes Fire?
NET Remedies is the labeler of record for Fire.

What form does Fire come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Fire prescription or over-the-counter?
The FDA label for this product is recorded as human prescription drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Has Fire been recalled?
4 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.