GOODSENSE TUSSIN CF MULTI-SYMPTOM COLD, RASPBERRY- dextromethorphan hbr, guaifenesin, phenylephrine hcl liquid

GoodSense Tussin CF Multi-Symptom Cold, Raspberry by

Drug Labeling and Warnings

GoodSense Tussin CF Multi-Symptom Cold, Raspberry by is a Otc medication manufactured, distributed, or labeled by Geiss, Destin & Dunn Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients (in each 5 mL or 1 teaspoon) Purposes
Dextromethorphan HBr, 10 mg........................................................ Cough Suppressant
Guaifenesin, 100 mg................................................................................... Expectorant
Phenylephrine HCI, 5 mg................................................................ Nasal Decongestant

PURPOSE

Purposes
Cough Suppressant
Expectorant
Nasal Decongestant

INDICATIONS & USAGE

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

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 DOCTOR

Ask a doctor before use if you have heart disease high blood pressure
thyroid disease diabete s 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 DOCTOR/PHARMACIST

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

OVERDOSAGE

Do not exceed recommended dosage.

STOP USE

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 persistant headache.
These could be signs of a serious condition.

PREGNANCY OR BREAST FEEDING

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

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

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 measure
only with dosing cup provided keep dosing cup with product TSP= teaspoon

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

OTHER SAFETY INFORMATION

Other information
each teaspoon (5mL) contains: sodium 3 mg
store at 15-30°C (59-86°F ). Do not refrigerate.

INACTIVE INGREDIENT

Inactive ingredients anhydrous citric acid, FD&C red #40, glycerin, propylene
glycol, purified water, raspberry flavor, sodium benzoate, sorbitol solution, sucralose

QUESTIONS

Questions or comments? 1-888-446-4753 Monday - Friday from
8 AM - 5 PM Eastern Standard Time.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GOODSENSE TUSSIN CF MULTI-SYMPTOM COLD, RASPBERRY 
dextromethorphan hbr, guaifenesin, phenylephrine hcl liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50804-256
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV)	PHENYLEPHRINE HYDROCHLORIDE	5 mg  in 5 mL
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	10 mg  in 5 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	100 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
FD&C RED NO. 40 (UNII: WZB9127XOA)
SORBITOL SOLUTION 70% (UNII: 8KW3E207O2)
SUCRALOSE (UNII: 96K6UQ3ZD4)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Product Characteristics
Color		Score
Shape		Size
Flavor	RASPBERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50804-256-04	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/05/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	11/05/2024

Labeler - Geiss, Destin & Dunn Inc. (076059836)

Registrant - Geiss, Destin & Dunn Inc. (076059836)