ROBITUSSIN HONEY MAXIMUM STRENGTH COUGH AND CHEST CONGESTION DM- dextromethorphan hbr, guaifenesin solution 
Haleon US Holdings LLC

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Drug Facts

Drug Facts

Active ingredients (in each 20 ml)Purposes

Dextromethorphan HBr, USP 20 mg

Cough suppressant

Guaifenesin, USP 400 mg

Expectorant

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 useif 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 ifcough 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 over

20 ml every 4 hours

children under 12 years

do 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 US

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

  1. Controls Cough
  2. Relieves Chest Congestion
  3. Thins & Loosens Mucus

Taste the
Real Honey

DM
MAX

For Ages 12+
4 FL OZ (118 ml)

Robitussin Honey C+CC DM Max 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 AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 mg  in 20 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN400 mg  in 20 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
SODIUM GLUCONATE (UNII: R6Q3791S76)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
ZINC GLUCONATE (UNII: U6WSN5SQ1Z)  
HONEY (UNII: Y9H1V576FH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0031-8756-121 in 1 CARTON06/25/2018
1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:0031-8756-181 in 1 CARTON06/25/2018
2237 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01206/25/2018
Labeler - Haleon US Holdings LLC (079944263)

Revised: 3/2024
Document Id: 13f96484-7b0e-10b3-e063-6294a90a7156
Set id: eaa10aed-5b1e-48bf-bc05-7a5638851daf
Version: 7
Effective Time: 20240318
 
Haleon US Holdings LLC