Drugplain

GUNA-COUGH 1 [hp_X]/150mL

ALTHAEA OFFICINALIS LEAF - ANTIMONY POTASSIUM TARTRATE - BRYONIA ALBA ROOT - CETRARIA ISLANDICA SUBSP. ISLANDICA - COCHINEAL - COPPER - DROSERA ROTUNDIFOLIA - ECHINACEA ANGUSTIFOLIA - GARDEN THYME - LOBARIA PULMONARIA - PLANTAGO MAJOR - · SOLUTION/ DROPS · Guna spa

No Recall History
Plain English

GUNA-COUGH is a solution/ drops containing althaea officinalis leaf - antimony potassium tartrate - bryonia alba root - cetraria islandica subsp. islandica - cochineal - copper - drosera rotundifolia - echinacea angustifolia - garden thyme - lobaria pulmonaria - plantago major - at 1 [hp_X]/150mL, taken oral. Manufactured by Guna spa.

Key Facts

Brand Name
GUNA-COUGH
Generic Name
ALTHAEA OFFICINALIS LEAF - ANTIMONY POTASSIUM TARTRATE - BRYONIA ALBA ROOT - CETRARIA ISLANDICA SUBSP. ISLANDICA - COCHINEAL - COPPER - DROSERA ROTUNDIFOLIA - ECHINACEA ANGUSTIFOLIA - GARDEN THYME - LOBARIA PULMONARIA - PLANTAGO MAJOR -
NDC Code (Product)
17089-453
Manufacturer
Guna spa
Strength
1 [hp_X]/150mL
Dosage Form
SOLUTION/ DROPS
Route
ORAL
Marketing Status
Drug Class
Copper-containing Intrauterine Device [EPC]; Non-Standardized Food Allergenic Extract [EPC]
Marketing Start
05/27/2010

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Directions: use enclosed cup for dosing.

Dosage & Administration

DIRECTIONS Use enclosed dosage cup for dosing Adults and children 12 years and older 10 ml every 4 hours as needed Children between 12 years and 2 years of age 5 ml every 4 hours as needed Children under 2 years Ask a physician

Warnings

WARNINGS Ask a doctor before use if you have a persistent or chronic cough that lasts, is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema or is accompanied by excessive phlegm (mucus). Stop use and ask a doctor if cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of a serious illness. If pregnant or breast-feeding ask a health care professional before use. Keep out of reach of children. In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately

Frequently Asked Questions

What is GUNA-COUGH used for?

GUNA-COUGH contains ALTHAEA OFFICINALIS LEAF - ANTIMONY POTASSIUM TARTRATE - BRYONIA ALBA ROOT - CETRARIA ISLANDICA SUBSP. ISLANDICA - COCHINEAL - COPPER - DROSERA ROTUNDIFOLIA - ECHINACEA ANGUSTIFOLIA - GARDEN THYME - LOBARIA PULMONARIA - PLANTAGO MAJOR -. It is a solution/ drops taken oral. Consult your doctor for specific uses.

Is GUNA-COUGH a controlled substance?

GUNA-COUGH is not classified as a controlled substance by the DEA.

What is the generic name for GUNA-COUGH?

The generic name for GUNA-COUGH is ALTHAEA OFFICINALIS LEAF - ANTIMONY POTASSIUM TARTRATE - BRYONIA ALBA ROOT - CETRARIA ISLANDICA SUBSP. ISLANDICA - COCHINEAL - COPPER - DROSERA ROTUNDIFOLIA - ECHINACEA ANGUSTIFOLIA - GARDEN THYME - LOBARIA PULMONARIA - PLANTAGO MAJOR -. There are no other listed brand versions of ALTHAEA OFFICINALIS LEAF - ANTIMONY POTASSIUM TARTRATE - BRYONIA ALBA ROOT - CETRARIA ISLANDICA SUBSP. ISLANDICA - COCHINEAL - COPPER - DROSERA ROTUNDIFOLIA - ECHINACEA ANGUSTIFOLIA - GARDEN THYME - LOBARIA PULMONARIA - PLANTAGO MAJOR -.

What is the NDC code for GUNA-COUGH 1 [hp_X]/150mL?

The NDC (National Drug Code) for GUNA-COUGH 1 [hp_X]/150mL is 17089-453, listed by Guna spa.

Product NDC

17089-453

Package NDC

17089-453-24

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)