Metal

ALUMINIA, AMMON CARB, ANACARDIUM, ANTIMON CRUD, HYDRASTIS, IGNATIA, MAG PHOS, NAT MUR, NITRICUM AC, OSMIUM, PARAFFINUM, SENNA, SILICEA, SPONGIA ORAL HUMAN OTC DRUG

Metal is an FDA drug label for the active ingredient ALUMINIA, AMMON CARB, ANACARDIUM, ANTIMON CRUD, HYDRASTIS, IGNATIA, MAG PHOS, NAT MUR, NITRICUM AC, OSMIUM, PARAFFINUM, SENNA, SILICEA, SPONGIA 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
ALUMINIA, AMMON CARB, ANACARDIUM, ANTIMON CRUD, HYDRASTIS, IGNATIA, MAG PHOS, NAT MUR, NITRICUM AC, OSMIUM, PARAFFINUM, SENNA, SILICEA, SPONGIA
Manufacturer
NET Remedies
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
61626-0103
Application
N/A
Label effective
20210119

About this product

Metal is an FDA-registered drug product whose active ingredient is ALUMINIA, AMMON CARB, ANACARDIUM, ANTIMON CRUD, HYDRASTIS, IGNATIA, MAG PHOS, NAT MUR, NITRICUM AC, OSMIUM, PARAFFINUM, SENNA, SILICEA, SPONGIA. It is labelled by NET Remedies taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 61626-0103, 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 ALUMINIA, AMMON CARB, ANACARDIUM, ANTIMON CRUD, HYDRASTIS, IGNATIA, MAG PHOS, NAT MUR, NITRICUM AC, OSMIUM, PARAFFINUM, SENNA, SILICEA, SPONGIA are most often described in connection with: temporary relief, neuro-emotional autonomic, nervous system, non psychiatric, disorders grief, dogmatically positioned, sadness crying, related emotions. 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: Aluminia, Ammon carb, Anacardium, Antimon crud, Hydrastis, Ignatia, Mag phos, Nat mur, Nitricum ac, Osmium, Paraffinum, Senna, Silicea, Spongia. (*) The letters "HPUS" indicate that the components in the product are officially monographed in the Homeopathic Pharmacopeia of the United States. (**) Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Indications & Usage

​INDICATIONS FOR USE: For the temporary relief of the neuro-emotional (autonomic nervous system - non psychiatric) disorders of grief, dogmatically positioned, sadness, crying, and related emotions. Sensory, spinal and extremity disorders. Nose - smell, mucous. Constipation. Skin - dry, itching. Weak spine disorders.**

Dosage & Administration

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

Warnings

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

Recall and safety notices

5 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-0576-2024 Little Moon Essentials, Ass Kisser, Packaged as a) 0.5 OZ (14G) metal tin, UPC Code 6 73673 88228 2, NDC 70722-208-05; b) 3 OZ (85.05G) metal tin, UPC Code 6 73673 88208 4, NDC 70722-208-03; Little Moon Essentials LLC Dania Beach, Fl 33004 Little Moon Essentials LLC Class II Ongoing 20240710
D-0577-2024 Little Moon Essentials, Asana Kisser, (Camphor 1.35%, Menthol 2.86%), Packaged as a) 0.5 OZ (14G) metal tin, UPC Code 6 73673 88227 5, NDC 70722-216-05; b) 3 OZ (85-05G) metal tin UPC Code 6 73673 88216 9, NDC 70722-216-03; Little Moon Essentials LLC Dania Beach, Fl 33004 Little Moon Essentials LLC Class II Ongoing 20240710
D-0575-2024 Little Moon Essentials, Vital Vapor Balm, (Camphor 0.6%, Menthol 5.2%) Packaged as a) 0.5OZ (14G) metal tin, UPC Code 6 73673 88231 2, NDC 70722-229-05) b) 2OZ (57G) glass jar, UPC Code 6 73673 88220 6, NDC 70722-229-02; c) 4OZ (113G) glass jar, UPC Code 6 73673 88218 3, NDC 70722-229-04; Little Moon Essentials LLC Dania Beach, Fl 33004 Little Moon Essentials LLC Class II Ongoing 20240710
D-0573-2024 Little Moon Essentials, Aching Head Rub (Camphor 3.09%, Menthol 2.55%) , a) 0.5OZ (14G), metal tin, UPC Code 67367388226 8, NDC 70722-203-05; b)1OZ (28G) glass jar, UPC Code 6 73673 88203 9, NDC 70722-203-01; Little Moon Essentials LLC Dania Beach, Fl 33004 Little Moon Essentials LLC Class II Ongoing 20240710
D-0448-2023 Unguentine Original Ointment for Burns (Camphor 3.0%, Phenol 2.5%, Tannic Acid 2.2%, Oxide 6.6%) packaged in 1 oz. (28g) metal tubes, Distributed by: Oakhurst Company Levittown, NY 11756 Ecometics, Inc. Class II Terminated 20230315

Frequently asked questions

What is Metal used for?
​INDICATIONS FOR USE: For the temporary relief of the neuro-emotional (autonomic nervous system - non psychiatric) disorders of grief, dogmatically positioned, sadness, crying, and related emotions. Sensory, spinal and extremity disorders. Nose - smell, mucous. Constipation. Skin - dry, itching. Weak spine disorders.**

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

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

Has Metal been recalled?
5 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.