TUKOL COUGH AND COLD HONEY FLAVOR- dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride syrup

Tukol Cough And Cold Honey Flavor by

Drug Labeling and Warnings

Tukol Cough And Cold Honey Flavor by is a Otc medication manufactured, distributed, or labeled by Genomma Lab USA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

ACTIVE INGREDIENT

Active ingredients (in each 5 mL tsp)	Purpose
Dextromethorphan HBr,10 mg	Cough Suppressant
Guaifenesin, 100 mg	Expectorant
Phenylephrine HCl, 5 mg	Nasal Decongestant

Uses

• helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes
• temporarily relieves these symptoms occurring with a cold:
  • nasal congestion
  • cough due to minor throat and bronchial irritation

Warnings

Do not use if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask a doctor before use if you have

• heart disease
• high blood pressure
• thyroid disease
• diabetes
• trouble urinating due to an enlarged prostate gland
• cough that occurs with too much phlegm (mucus)
• cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema

Ask a doctor or pharmacist before use if you are taking any other oral nasal decongestant or stimulant

Do not exceed recommended dosage

Stop use and ask a doctor if

• you get nervous, dizzy or sleepless
• symptoms do not get better within 7 days or are accompanied by fever
• cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

• do not take more than 6 doses in any 24 hour period
• this adult strength product is not intended for use in children under 12 years of age

age	dose
adults and children 12 years and over	2 teaspoons (10 mL) every 4 hours
children under 12	do not use

Other information

• each teaspoon contains: sodium 3 mg
• store at 20-25°C (68-77°F). Do not refrigerate
• dosage cup provided

Inactive ingredients

anhydrous citric acid, FD&C yellow # 6, flavor, glycerin, honey, propylene glycol, purified water, sodium benzoate, sorbitol solution, sucralose, xanthan gum

Questions or comments?

1-877-99 GENOM (43666)
Monday to Friday from 8 am to 6 pm, Central time.

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Distributed by: Genomma Lab USA Inc., Houston, TX, 77027

PRINCIPAL DISPLAY PANEL - 118 ml Bottle Carton

Dextromethorphan HBr / Guaifenesin / Phenylephrine HCl

Tukol®

X-PECTO HONEY

COUGH & COLD

• Quiets Cough
• Thins & loosens Phlegm
• Clears Nasal Congestion

NATURAL HONEY FLAVOR

Ages 12+
4 FL OZ (118 ml)

INGREDIENTS AND APPEARANCE

TUKOL COUGH AND COLD HONEY FLAVOR 
dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride syrup

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50066-534
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Dextromethorphan Hydrobromide (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	Dextromethorphan Hydrobromide	2 mg  in 1 mL
Guaifenesin (UNII: 495W7451VQ) (Guaifenesin - UNII:495W7451VQ)	Guaifenesin	20 mg  in 1 mL
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV)	PHENYLEPHRINE HYDROCHLORIDE	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
Propylene Glycol (UNII: 6DC9Q167V3)
Sorbitol (UNII: 506T60A25R)
Sucralose (UNII: 96K6UQ3ZD4)

Product Characteristics
Color	YELLOW (Amber to yellow)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50066-534-04	1 in 1 CARTON	09/20/2019
1		118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	09/20/2019

Labeler - Genomma Lab USA (832323534)