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 -

FDA Drug Profile — GUNA-COUGH

Drug Details

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 -
Brand Names
GUNA-COUGH
Application Number
Sponsor
Guna spa
NDC Codes
1
Dosage Forms
SOLUTION/ DROPS
Routes
ORAL
Active Ingredients
ALTHAEA OFFICINALIS LEAF, ANTIMONY POTASSIUM TARTRATE, BRYONIA ALBA ROOT, CETRARIA ISLANDICA SUBSP. ISLANDICA, COCHINEAL, COPPER, DROSERA ROTUNDIFOLIA, ECHINACEA ANGUSTIFOLIA, LOBARIA PULMONARIA, PLANTAGO MAJOR, THYME

Indications and Usage

Directions: use enclosed cup for dosing.

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