GOODMEDS NON-DROWSY COUGH RELIEF- dextromethorphan hydrobromide capsule, liquid filled

Goodmeds Non-Drowsy Cough Relief by

Drug Labeling and Warnings

Goodmeds Non-Drowsy Cough Relief by is a Otc medication manufactured, distributed, or labeled by Cabinet Health P.B.C., ELYSIUM PHARMACEUTICALS LIMITED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient (in each softgel)

Dextromethorphan HBr, 15 mg

Purpose

Cough suppressant

Uses

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

Warnings

Do not use

if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (cenain drugs for depression, psychiatric, cr emotional conditions, or Parkinson's disease), cr 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

a cough that occurs with too much phlegm (mucus)
a cough that lasts or is chronic as occurs with smoking, asthma, or emphysema

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.

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. (1-800-222-1222)

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

• age: dose
• adults and children 12 years and over: take 2 softgels every 6 to 8 hours, as needed
• children under 12 years: do not use

Other information

store at 20-25ºC (68-77ºF)
avoid excessive heat above 40ºC (104ºF)
protect from light

Inactive ingredients

FD&C red #40, gelatin, glycerin, polyethylene glycol 400, propylene glycol, povidone, purified water, sorbitol sorbitan solution. titanium dioxide

Questions or Comments?

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

Package Labeling:

INGREDIENTS AND APPEARANCE

GOODMEDS NON-DROWSY COUGH RELIEF 
dextromethorphan hydrobromide capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82725-4010
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	15 mg

Inactive Ingredients
Ingredient Name	Strength
FD&C RED NO. 40 (UNII: WZB9127XOA)
GELATIN (UNII: 2G86QN327L)
GLYCERIN (UNII: PDC6A3C0OX)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POVIDONE (UNII: FZ989GH94E)
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
SORBITAN (UNII: 6O92ICV9RU)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	red	Score	no score
Shape	OVAL	Size	7mm
Flavor		Imprint Code	904
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82725-4010-1	120 in 1 BOTTLE; Type 0: Not a Combination Product	10/10/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	10/10/2025

Labeler - Cabinet Health P.B.C. (117102391)

Registrant - Cabinet Health P.B.C. (117102391)

Establishment
Name	Address	ID/FEI	Business Operations
ELYSIUM PHARMACEUTICALS LIMITED		915664486	manufacture(82725-4010)