GoodSense Tussin CF Multi-Symptom Cold, Raspberry

Manufacturer
Geiss, Destin & Dunn Inc.
Effective date
2025-09-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:14:15

Label at a glance#

ProductGoodSense Tussin CF Multi-Symptom Cold, Raspberry
Active ingredientPHENYLEPHRINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN
Label structure15 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

Purposes
Cough Suppressant
Expectorant
Nasal Decongestant

INDICATIONS & USAGE SECTION

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 SECTION

Warnings

OTC - DO NOT USE SECTION

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.

OTC - ASK DOCTOR SECTION

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

OTC - ASK DOCTOR/PHARMACIST SECTION

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

OVERDOSAGE SECTION

Do not exceed recommended dosage.

OTC - STOP USE SECTION

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.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

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 over2 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 SECTION

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

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GoodSense Tussin CF RaspberryGoodSense Tussin CF Raspberry

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1044949dextromethorphan HBr 20 MG / guaiFENesin 200 MG / phenylephrine HCl 10 MG in 10 mL Oral SolutionPSN1
1044949dextromethorphan hydrobromide 2 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 1 MG/ML Oral SolutionSCD1
1044949dextromethorphan HBr 10 MG / guaifenesin 100 MG / phenylephrine HCl 5 MG per 5 ML Oral SolutionSY1
1044949dextromethorphan HBr 20 MG / guaifenesin 200 MG / phenylephrine HCl 10 MG per 10 ML Oral SolutionSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DEXTROMETHORPHAN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
GUAIFENESIN Pharmacologic Class Indexing1Indexing - Pharmacologic Class20211129
PHENYLEPHRINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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bf324df6-7127-7deb-def5-2681c136cd03Product name320250325
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e5b5c132-b15d-435b-9faa-2f74e5cadcf9Product name820250220
f489e8f3-5c9e-4818-b539-a73587edcfc7Product name220240229
0f7ae452-206d-4fc4-868d-56fc47074084Product name120231011
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e949165d-714d-e548-2b76-0cb5def16f30Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50804-256-04GoodSense Tussin CF Multi-Symptom Cold, Raspberry118 mL in 1 BOTTLELIQUID1181

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50804-25650804-256-04

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
GoodSense Tussin CF Multi-Symptom Cold, RaspberryDEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCLGeiss, Destin & Dunn Inc.3f05cf84-d485-7688-e063-6394a90ae7402025-09-17WarningsExact identifier
ndc (package): 50804-256-04
ndc (product): 50804-256
ndc11 (package): 50804025604
spl id: 3f05cf84-d486-7688-e063-6394a90ae740
spl set id: 3f05cf84-d485-7688-e063-6394a90ae740

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.