Cold Comfort Cold and Cough
Cold Comfort Cold and Cough is an FDA drug label for the active ingredient ALLIUM CEPA 5C, EUPHRASIA OFFICINALIS 5C, HYDRASTIS CANADENSIS 5C, NUX VOMICA 5C, PULSATILLA 5C, RUMEX CRISPUS 5C,SABADILLA 5C, SAMBUCUS NIGRA 5C manufactured by SEVENE USA administered by BUCCAL. 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 20260818.
- Generic name
- ALLIUM CEPA 5C, EUPHRASIA OFFICINALIS 5C, HYDRASTIS CANADENSIS 5C, NUX VOMICA 5C, PULSATILLA 5C, RUMEX CRISPUS 5C,SABADILLA 5C, SAMBUCUS NIGRA 5C
- Manufacturer
- SEVENE USA
- Product type
- HUMAN OTC DRUG
- Route
- BUCCAL
- Dosage form
- N/A
- NDC
- 76472-7003
- Application
- N/A
- Label effective
- 20260818
About this product
Cold Comfort Cold and Cough is an FDA-registered drug product whose active ingredient is ALLIUM CEPA 5C, EUPHRASIA OFFICINALIS 5C, HYDRASTIS CANADENSIS 5C, NUX VOMICA 5C, PULSATILLA 5C, RUMEX CRISPUS 5C,SABADILLA 5C, SAMBUCUS NIGRA 5C. It is labelled by SEVENE USA taken by buccal and marketed as a human otc drug product. Identifiers on file: NDC 76472-7003, label effective 20260818. 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 5C, EUPHRASIA OFFICINALIS 5C, HYDRASTIS CANADENSIS 5C, NUX VOMICA 5C, PULSATILLA 5C, RUMEX CRISPUS 5C,SABADILLA 5C, SAMBUCUS NIGRA 5C are most often described in connection with: runny nose, watery eyes, allium cepa, clear discharge, euphrasia officinalis, irritating eye, hydrastis canadensis, postnasal drip. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
USE ALLIUM CEPA Runny Nose with Clear Discharge - Sneezing - Watery Eyes .* EUPHRASIA OFFICINALIS Allergies with Abundant and Irritating Eye Discharge .* HYDRASTIS CANADENSIS Postnasal Drip - Stomach Ache with Constipation .* NUX VOMICA Indigestion, Heartburn, Drowsiness, Nausea from Overindulgence/Overeating .* PULSATILLA Ocular or Nasal Yellow Discharge Associated with Cold .* RUMEX CRISPUS Dry, Tickling, Persistent Cough Worsened by Cold Air .* SABADILLA Allergic Rhinitis (Hay Fever): Frequent Sneezing, Runny Nose, Nasal Itching, and Watery Eyes .* SAMBUCUS NIGRA Respiratory Disorders: Nasal congestion - Spasmodic/Suffocative Cough (nocturnal) - Croup - Asthma-like breathing difficulties .*
Dosage & Administration
DIRECTIONS Adults/Children above 6 : spray 2 shots directly under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.
Warnings
WARNINGS Consult a physician for use in children under 6 years of age. Contact a doctor if symptoms persist.
Frequently asked questions
What is Cold Comfort Cold and Cough used for?
USE ALLIUM CEPA Runny Nose with Clear Discharge - Sneezing - Watery Eyes .* EUPHRASIA OFFICINALIS Allergies with Abundant and Irritating Eye Discharge .* HYDRASTIS CANADENSIS Postnasal Drip - Stomach Ache with Constipation .* NUX VOMICA Indigestion, Heartburn, Drowsiness, Nausea from Overindulgence/Overeating .* PULSATILLA Ocular or Nasal Yellow Discharge Associated with Cold .* RUMEX CRISPUS …
Who makes Cold Comfort Cold and Cough?
SEVENE USA is the labeler of record for Cold Comfort Cold and Cough.
What form does Cold Comfort Cold and Cough come in?
administered by buccal. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Cold Comfort Cold and Cough 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 Comfort Cold and Cough 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.