GUNA-COUGH- 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-COUGH by

Drug Labeling and Warnings

GUNA-COUGH by is a Homeopathic medication manufactured, distributed, or labeled by Guna spa. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS/PURPOSE

ALTHAEA OFFICINALIS    1X    EXPECTORANT
ANTIMONIUM TARTARICUM    8X    ANTITUSSIVE, DRY COUGH
BRYONIA ALBA                6X    ANTI-INFLAMMATORY
CETRARIA ISLANDICA      4X    EXPECTORANT
COCCUS CACTI                6X    ANTITUSSIVE, WET COUGH
CUPRUM ACETICUM        8X    PAIN RELIEF
DROSERA                       1X    COUGH SUPPRESSANT, SPASMODIC COUGH
ECHINACEA ANGUSTIFOLIA    1X    IMMUNE SUPPORT
PLANTAGO MAJOR        1X    EXPECTORANT
STICTA PULMONARIA    4X    ANTITUSSIVE
THYME                          1X    EXPECTORANT

USES

Temporary relief of cough due to:

• Cold and flu
• Inhalation of irritants
• Excess mucus and phlegm

WARNINGS

Ask a doctor before use if you have persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema, or a cough accompanied by too much 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.

PREGNANCY

If pregnant or breast-feeding ask a doctor before use

WARNINGS

Keep this and all medicines out of reach of children

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

QUESTIONS

Questions?: info@gunainc.com
Tel. (484) 223-3500

INDICATIONS & USAGE

Directions: use enclosed cup for dosing.

INACTIVE INGREDIENT

Inactive ingredients: Cherry flavor, Fructose syrup, Hydroxypropyl methylcellulose, Potassium sorbate, purified water, Sodium benzoate.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GUNA-COUGH 
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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 17089-453
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALTHAEA OFFICINALIS LEAF (UNII: E2QQV92338) (ALTHAEA OFFICINALIS LEAF - UNII:E2QQV92338)	ALTHAEA OFFICINALIS LEAF	1 [hp_X]  in 150 mL
ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5)	ANTIMONY POTASSIUM TARTRATE	8 [hp_X]  in 150 mL
BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B)	BRYONIA ALBA ROOT	6 [hp_X]  in 150 mL
CETRARIA ISLANDICA SUBSP. ISLANDICA (UNII: BJ7YPN79A1) (CETRARIA ISLANDICA SUBSP. ISLANDICA - UNII:BJ7YPN79A1)	CETRARIA ISLANDICA SUBSP. ISLANDICA	4 [hp_X]  in 150 mL
COCHINEAL (UNII: TZ8Z31B35M) (COCHINEAL - UNII:TZ8Z31B35M)	COCHINEAL	6 [hp_X]  in 150 mL
COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5)	COPPER	8 [hp_X]  in 150 mL
DROSERA ROTUNDIFOLIA (UNII: 75O014T1HG) (DROSERA ROTUNDIFOLIA - UNII:75O014T1HG)	DROSERA ROTUNDIFOLIA	1 [hp_X]  in 150 mL
ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (ECHINACEA ANGUSTIFOLIA - UNII:VB06AV5US8)	ECHINACEA ANGUSTIFOLIA	1 [hp_X]  in 150 mL
PLANTAGO MAJOR (UNII: W2469WNO6U) (PLANTAGO MAJOR - UNII:W2469WNO6U)	PLANTAGO MAJOR	1 [hp_X]  in 150 mL
LOBARIA PULMONARIA (UNII: D1YM0P5Z2T) (LOBARIA PULMONARIA - UNII:D1YM0P5Z2T)	LOBARIA PULMONARIA	4 [hp_X]  in 150 mL
THYME (UNII: CW657OBU4N) (THYME - UNII:CW657OBU4N)	THYME	1 [hp_X]  in 150 mL

Inactive Ingredients
Ingredient Name	Strength
FRUCTOSE (UNII: 6YSS42VSEV)	22.5 mL  in 150 mL
HYPROMELLOSES (UNII: 3NXW29V3WO)	2.25 mL  in 150 mL
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)	0.15 mL  in 150 mL
SODIUM BENZOATE (UNII: OJ245FE5EU)	0.15 mL  in 150 mL

Product Characteristics
Color		Score
Shape		Size
Flavor	CHERRY (SOUR BLACK CHERRY)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 17089-453-24	1 in 1 BOX	04/09/2018
1		150 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		05/27/2010

Labeler - Guna spa (430538264)

Establishment
Name	Address	ID/FEI	Business Operations
Guna spa		338587646	manufacture(17089-453)