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Mucus relief - Medication Information

Product NDC Code 62795-1012
Drug Name

Mucus relief

Type Brand
Active Ingredients
Anemone hepatica var. obtusa 6 [hp_x]/1
Antimony potassium tartrate 5 [hp_x]/1
Atropa belladonna 6 [hp_x]/1
Bryonia alba whole 6 [hp_x]/1
Human sputum, bordetella pertussis infected 30 [hp_x]/1
Hyoscyamus niger 5 [hp_x]/1
Ipecac 6 [hp_x]/1
Lobaria pulmonaria 5 [hp_x]/1
Lobelia inflata 4 [hp_x]/1
Route ORAL
Dosage Form TABLET
Labeler Name MediNatura Inc
Packages
Package NDC Code Description
62795-1012-2 100 tablet in 1 bottle (62795-1012-2)
62795-1012-3 1 bottle in 1 carton (62795-1012-3) / 100 tablet in 1 bottle
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
ACTIVE INGREDIENT Each tablet contains: Antimonium tartaricum 5X, *Belladonna 6X, *Bryonia alba 6X, *Hepatica triloba 6X, *Hyoscyamus niger 5X, *Ipecacuanha 6X, *Lobelia inflata 4X, *Pertussinum 30X, *Sticta pulmonaria 5X 33.3 mg each. *Natural Ingredients

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
DIRECTIONS At first sign of symptoms: Adults and children 4 years and older: 1 tablet every 1/2 to 1 hour until symptoms lessen, then continue with standard dosage. Standard dosage: Adults and children 4 years and older : Take 1-2 tablets every 4 to 6 hours. Do not exceed 12 tablets in 24 hours. For children under 4, consult your health professional. Allow tablets to dissolve completely in the mouth, do not swallow.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
INACTIVE INGREDIENT Inactive Ingredients: Dextrose, Magnesium Stearate, Maltodextrin

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses: For the temporary relief of minor chest congestion and cough due to mucus build-up

Purpose

Information about the drug product’s indications for use.
PURPOSE Mucus Relief Tablets Relieves: • Chest Congestion • Mucus Build-up • Cough

Spl product data elements

Usually a list of ingredients in a drug product.
Mucus Relief ANTIMONY POTASSIUM TARTRATE, ATROPA BELLADONNA, BRYONIA ALBA WHOLE, ANEMONE AMERICANA, HYOSCYAMUS NIGER, IPECAC, LOBELIA INFLATA, HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED, and LOBARIA PULMONARIA ANTIMONY POTASSIUM TARTRATE ANTIMONY CATION (3+) ATROPA BELLADONNA ATROPA BELLADONNA BRYONIA ALBA WHOLE BRYONIA ALBA WHOLE ANEMONE HEPATICA VAR. OBTUSA ANEMONE HEPATICA VAR. OBTUSA HYOSCYAMUS NIGER HYOSCYAMUS NIGER IPECAC IPECAC LOBELIA INFLATA LOBELIA INFLATA HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED LOBARIA PULMONARIA LOBARIA PULMONARIA MAGNESIUM STEARATE MALTODEXTRIN DEXTROSE Leafman

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Add image transcription here... BHI Mucus Tablet

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
KEEP OUT OF REACH OF CHILDREN Keep out of reach of children.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
WARNINGS

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API