GOODMEDS COUGH RELIEF DEXTROMETHORPHAN HBR - Cabinet Health P.B.C.

Manufacturer
Cabinet Health P.B.C.
Effective date
2026-10-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-10-10 01:02:44

Label at a glance#

ProductGOODMEDS COUGH RELIEF DEXTROMETHORPHAN HBR
Active ingredientDEXTROMETHORPHAN HYDROBROMIDE
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Dextromethorphan HBr 15mg

OTC - PURPOSE SECTION

Cough Suppressant

INDICATIONS & USAGE SECTION

Use

temporarily relieves cough due to minor throat
and bronchial irritation as may occur with a cold.

WARNINGS SECTION

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.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have
■ a cough that occurs with too much phlegm (mucus)
■ a cough that lasts or is chronic as occurs with
smoking, asthma, or emphysema

OTC - STOP USE SECTION

Stop use and ask a doctor if cough lasts for more than 7 days, comes back, or is accompanied by fever, rash, or persistent 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. (1-800-222-1222)

DOSAGE & ADMINISTRATION SECTION

Directions
■ do not take more than 8 softgels in any 24-hour period
■ this adult product is not intended for use in children under 12 years of age

agedose
adults and children 12 years and overtake 2 softgels every 6 to 8 hours, as needed
children under 12 yearsdo not use

OTHER SAFETY INFORMATION

Other information
■ store at 20–25°C (68–77°F)
■ avoid excessive heat above 40°C (104°F)
■ protect from light

INACTIVE INGREDIENT SECTION

Inactive ingredients
FD&C blue #1, FD&C red #40, gelatin, glycerin, polyethylene glycol, povidone K30, propyl gallate, propylene glycol, purified water, sorbitol sorbitan solution

OTC - QUESTIONS SECTION

Questions or comments?
call 1-908-242-6108 Mon-Fri 8:00 AM to 5:00 PM EST

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principle Display Panel

PDPPDP

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData MatrixGM-4110-3-DF ORG 09 2026GM CoughRelief 240ct.jpg

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82725-411082725-4110-1, 82725-4110-2, 82725-4110-3

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-04-20full-release2026-06-01 01:54:40

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
4fe96742-b2b2-55f3-e063-6294a90a04a8aeb26c0e-4efe-4099-9b68-47824f4506c02026-04-20WarningsExact identifier
spl set id: aeb26c0e-4efe-4099-9b68-47824f4506c0

Reported adverse events (FAERS/openFDA)#

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