G-TUSS-NL- dextromethorphan hydrobromide, guaifenesin, and pseudoephedrine hydrochloride liquid

G-Tuss-NL by

Drug Labeling and Warnings

G-Tuss-NL by is a Otc medication manufactured, distributed, or labeled by McLaren Medical, davAgen Pharmaceutical, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active Ingredients (in each 5 mL, teaspoonful)	Purpose
Guaifenesin 200 mg	Expectorant
Dextromethorphan HBr 10 mg	Cough Suppressant
Pseudoephedrine HCl 30 mg	Nasal Decongestant

Indications

• For the temporary relief of nasal congestion due to the common cold, hay fever or other upper respiratory allergies (allergic rhinitis).
• Helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive.
• Temporarily controls cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants.
• Temporarily helps you cough less.

Warnings

• Do not exceed recommended dosage.
  If nervousness, dizziness or sleeplessness occurs, discontinue use and consult a doctor.

• If symptoms do not improve within 7 days or are accompanied by fever, consult a doctor.

• Do not take this product if you have heart disease, high blood pressure, thyroid disease, diabetes or difficulty in urination due to enlargement of the prostate gland unless directed by a doctor.
• 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.

• A persistent cough may be the sign of a serious condition. If cough persists for more than 1 week, tends to recur or is accompanied by a fever, rash or persistent headache, consult a doctor.

• Do not take this product for persistent or chronic cough such as occurs with smoking, asthma or emphysema or if cough is accompanied by excessive phlegm (mucus) unless directed by a doctor.

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

• In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately.

• Keep this and all drugs out of the reach of children.

Directions

Do not take more than 6 doses in any 24-hour period.

• Adults and children 12 years of age and over: 2 teaspoonfuls (10 mL) every 4 hours
• Children 6 to under 12 years of age: 1 teaspoonful (5 mL) every 4 hours
• Children under 6 years of age: Consult a doctor

Inactive Ingredients

Citric Acid, Grape Flavor, Propylene Glycol, Purified Water, Saccharine Sodium, Sodium Benzoate, Sorbitol, Sucralose.

Other Information

Store at 20°-25°C (68°-77°F)

Tamper evident by seal under cap. Do not use if the seal is broken or missing.

PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label

NDC-43913-404-16

G-Tuss-NL

Cough Suppressant, Expectorant & Nasal Decongestant

Sugar Free Dye Free Alcohol Free Phenylalanine Free

Grape Flavor

16 FL OZ (473 mL)

Multiple Dose Unit Package
For Dispensing Under Pharmaceutical Supervision Only

McLaren Medical

INGREDIENTS AND APPEARANCE

G-TUSS-NL 
dextromethorphan hydrobromide, guaifenesin, and pseudoephedrine hydrochloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43913-404
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Dextromethorphan Hydrobromide (UNII: 9D2RTI9KYH) (Dextromethorphan - UNII:7355X3ROTS)	Dextromethorphan Hydrobromide	10 mg  in 5 mL
Guaifenesin (UNII: 495W7451VQ) (Guaifenesin - UNII:495W7451VQ)	Guaifenesin	200 mg  in 5 mL
Pseudoephedrine Hydrochloride (UNII: 6V9V2RYJ8N) (Pseudoephedrine - UNII:7CUC9DDI9F)	Pseudoephedrine Hydrochloride	30 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
Sodium Benzoate (UNII: OJ245FE5EU)
Citric Acid Monohydrate (UNII: 2968PHW8QP)
Sorbitol (UNII: 506T60A25R)
Saccharin Sodium (UNII: SB8ZUX40TY)
Sucralose (UNII: 96K6UQ3ZD4)
Propylene Glycol (UNII: 6DC9Q167V3)
Water (UNII: 059QF0KO0R)

Product Characteristics
Color		Score
Shape		Size
Flavor	GRAPE	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43913-404-16	473 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part341	02/11/2014

Labeler - McLaren Medical (013770591)

Registrant - davAgen Pharmaceutical, LLC (967545935)

Establishment
Name	Address	ID/FEI	Business Operations
davAgen Pharmaceutical, LLC		967545935	MANUFACTURE(43913-404) , PACK(43913-404) , LABEL(43913-404) , ANALYSIS(43913-404)