Cold Armor

ALLIUM CEPA, HYDRASTIS CANADENSIS, PULSATILLA (PRATENSIS), DULCAMARA, NUX VOMICA, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, KALI BICHROMICUM ORAL HUMAN OTC DRUG

Cold Armor is an FDA drug label for the active ingredient ALLIUM CEPA, HYDRASTIS CANADENSIS, PULSATILLA (PRATENSIS), DULCAMARA, NUX VOMICA, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, KALI BICHROMICUM manufactured by Ratis, LLC 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 20230526.

Generic name
ALLIUM CEPA, HYDRASTIS CANADENSIS, PULSATILLA (PRATENSIS), DULCAMARA, NUX VOMICA, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, KALI BICHROMICUM
Manufacturer
Ratis, LLC
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
71753-1156
Application
N/A
Label effective
20230526

About this product

Cold Armor is an FDA-registered drug product whose active ingredient is ALLIUM CEPA, HYDRASTIS CANADENSIS, PULSATILLA (PRATENSIS), DULCAMARA, NUX VOMICA, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, KALI BICHROMICUM. It is labelled by Ratis, LLC taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 71753-1156, label effective 20230526. 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 ALLIUM CEPA, HYDRASTIS CANADENSIS, PULSATILLA (PRATENSIS), DULCAMARA, NUX VOMICA, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, KALI BICHROMICUM are most often described in connection with: temporariy relieve, runny nose, coughing congestion, body aches, fever weakness, minor sore, throat claims, based traditional. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

ACTIVE INGREDIENTS: (in each drop) Allium Cepa 6X 12.50%, Hydrastis Canadensis 6X 12.50%, Pulsatilla Pratensis 6X 12.50%, Dulcamara 8x 12.50%, Nux Vomica 8x 12.50%, Ferrum Phosphoricum 12X 12.50%, Gelsemium Sempervirens 12X 12.50%, Kali Bichromicum 12X 12.50%

Indications & Usage

USES: May temporariy relieve stuffy and runny nose, coughing, congestion, body aches, fever, weakness, and minor sore throat.* * Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Dosage & Administration

DIRECTIONS: • Adults: 2 sprays 3 times a day or as needed • Children 3-6: 1 spray as above • Consult a physician for use in children under 6 years of age. Store in a cool, dry place

Warnings

WARNINGS: Sore throat warning: Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult a physician promptly. Do not use more than 2 days or administer to children under 3 years of age unless directed by a physician. Stop use and ask a doctor if symptoms persist for more than 2 days. For oral use only. If pregnant or breast-feeding, ask a health care professional 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 IS BROKEN OR MISSING

Frequently asked questions

What is Cold Armor used for?
USES: May temporariy relieve stuffy and runny nose, coughing, congestion, body aches, fever, weakness, and minor sore throat.* * Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Who makes Cold Armor?
Ratis, LLC is the labeler of record for Cold Armor.

What form does Cold Armor 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 Cold Armor 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 Cold Armor been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

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.