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Robitussin Honey Maximum Strength Cough and Chest Congestion DM

Medically reviewed by Drugs.com. Last updated on Oct 3, 2019.

Dosage form: solution
Ingredients: DEXTROMETHORPHAN HYDROBROMIDE 20mg in 20mL, GUAIFENESIN 400mg in 20mL
Labeler: Wyeth Consumer Healthcare LLC
NDC Code: 0031-8756

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Robitussin® Honey Maximum Strength Cough and Chest Congestion DM

Drug Facts

Active ingredients (in each 20 ml)Purposes
Dextromethorphan HBr, USP 20 mgCough suppressant
Guaifenesin, USP 400 mgExpectorant

Uses

  • temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold
  • helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes

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

Stop use and ask a doctor if cough lasts 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.

Directions

  • do not take more than 6 doses in any 24-hour period
  • measure only with dosing cup provided
  • keep dosing cup with product
  • ml = milliliter
  • this adult product is not intended for use in children under 12 years of age
agedose
adults and children 12 years and over20 ml every 4 hours
children under 12 yearsdo not use

Other information

  • each 20 ml contains: sodium 21 mg
  • store at 20-25°C (68-77°F). Do not refrigerate.

Inactive ingredients

anhydrous citric acid, carboxymethylcellulose sodium, glycerin, natural and artificial flavors, natural grade A honey, polyethylene glycol, propylene glycol, purified water, sodium benzoate, sodium citrate, sodium gluconate, sucralose, xanthan gum, zinc gluconate

Questions or comments?

call weekdays from 9 AM to 5 PM EST at 1-800-762-4675

Distributed by: Pfizer, Madison, NJ 07940 USA

PRINCIPAL DISPLAY PANEL - 118 ml Bottle Label

ADULT

Robitussin®

Honey

MAXIMUM STRENGTH

Cough+Chest
Congestion DM

DM
MAX

DEXTROMETHORPHAN HBr (Cough Suppressant)
GUAIFENESIN (Expectorant)

NON-DROWSY

4 FL OZ (118 ml)

PRINCIPAL DISPLAY PANEL - 118 ml Bottle Carton

ADULT

NEW!

Robitussin®

Honey

Cough+Chest
Congestion DM

DEXTROMETHORPHAN HBr (Cough Suppressant)
GUAIFENESIN (Expectorant)

NON-DROWSY

MAXIMUM STRENGTH

Controls Cough
Relieves Chest Congestion
Thins & Loosens Mucus

Taste the
Real Honey

DM
MAX

For Ages 12+
4 FL OZ (118 ml)

ROBITUSSIN HONEY MAXIMUM STRENGTH COUGH AND CHEST CONGESTION DM 
dextromethorphan hbr, guaifenesin solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0031-8756
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (DEXTROMETHORPHAN) DEXTROMETHORPHAN HYDROBROMIDE20 mg  in 20 mL
GUAIFENESIN (GUAIFENESIN) GUAIFENESIN400 mg  in 20 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID 
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM 
GLYCERIN 
POLYETHYLENE GLYCOL, UNSPECIFIED 
PROPYLENE GLYCOL 
WATER 
SODIUM BENZOATE 
SODIUM CITRATE, UNSPECIFIED FORM 
SODIUM GLUCONATE 
SUCRALOSE 
XANTHAN GUM 
ZINC GLUCONATE 
HONEY 
Packaging
#Item CodePackage Description
1NDC:0031-8756-121 BOTTLE in 1 CARTON
1118 mL in 1 BOTTLE
2NDC:0031-8756-181 BOTTLE in 1 CARTON
2237 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34106/25/2018
Labeler - Wyeth Consumer Healthcare LLC (828831730)
Establishment
NameAddressID/FEIOperations
PF Consumer Healthcare Canada ULC203812479ANALYSIS(0031-8756), LABEL(0031-8756), MANUFACTURE(0031-8756), PACK(0031-8756)

 
Wyeth Consumer Healthcare LLC