(DA) Resfridol Antitussive (NEW)

Resfridol by

Drug Labeling and Warnings

Resfridol by is a Otc medication manufactured, distributed, or labeled by Laboratorios Alfa. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

RESFRIDOL ANTITUSSIVE- dextromethorphan hbr, guaifenesin syrup 
Laboratorios Alfa

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(DA) Resfridol Antitussive (NEW)

Drug Facts

Active ingredients and Purposes

• Active ingredients (in each 10 mL): Purposes
• Dextromethorphan HBr 5 mg ............................................................................:

  Cough suppressant

• Guaifenesin 200 mg...........................................................................................: Expectorant

Uses

Temporarily relieves common cold symptoms:

• cough due to minor throat & bronchial irritation
• helps loosen phlegm (mucus) and thin bronchial secretions to:
• drain bronchial tubes
• make coughs more productive

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.

Stop use and ask a doctor if

■ a cough persists for more than 7 days, tends to recur, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.

Ask a doctor before use if you have

■a cough that is accompanied by excessive phlegm (mucus)

■ a persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of accidental overdose, get medical help or contact a Poison Control Center right away.

Directions

■ only use the dosage cup provided

■ shake well before use

■ do not exceed 6 doses per 24-hour period

• Age: Dose
• adults and children 12 years and older: 20 mL, every 4 hours
• children 6 to under 12 years: 10 mL, every 4 hours
• children under 6 years: do not use

Other information

■ store between 68-77°F (20-25°C)

■ do not use if safety seal over cap is torn, broken, or missing

Inactive ingredients

anhydrous citric acid, FD&C red #40, flavors, sodium benzoate, sorbitol, sucralose, water

Questions?

+1-809-544-0222

(M-F) 9 AM - 5 PM EST or www.laboratoriosalfa.com

Principal Display Panel

RESFRIDOL  ANTITUSSIVE
dextromethorphan hbr, guaifenesin syrup

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72483-101
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	5 mg  in 10 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	200 mg  in 10 mL

Inactive Ingredients
Ingredient Name	Strength
SUCRALOSE (UNII: 96K6UQ3ZD4)
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
FD&C RED NO. 40 (UNII: WZB9127XOA)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Product Characteristics
Color	red	Score
Shape		Size
Flavor	STRAWBERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72483-101-04	1 in 1 BOX	01/31/2026	01/31/2026
1		120 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	01/31/2026	01/31/2026

Labeler - Laboratorios Alfa (815941244)

Revised: 3/2026

Document Id: 4e5790cb-16b9-d6af-e063-6394a90ab2da

34390-5

Set id: 2864cc43-2213-c970-e063-6394a90ac61e

Version: 3

Effective Time: 20260331