Robitussin Medi-Soothers

The listing

NDC product code

0031-9306 (labeller 0031, product 9306)

Labeller

Haleon US Holdings LLC

Brand name

Robitussin Medi-Soothers

Generic name

dextromethorphan hydrobromide, menthol

Dosage form

Lozenge

Route

oral

Marketing category

OTC MONOGRAPH DRUG M012

Marketing start

1 June 2023

Listing expires

31 December 2026

RxNorm concept

1301246

Active ingredients

Strengths as listed in the FDA National Drug Code Directory, retrieved 4 September 2026. "Other listings" counts every other product on this site containing the same ingredient at any strength.

What the label claims

These are read from this product's own label, not assigned by us and not inferred from the ingredient.

Stated purposeCough suppressantOral anesthetic

Stated useSore throatMinor throat irritationCoughSore mouth, gums and canker soresCommon cold symptoms

Drug Facts, as filed

Quoted from the label FDA holds for this product. Long fields are truncated. The panel printed on the package you are holding is the one that governs.

Active ingredient

(in each lozenge) Dextromethorphan HBr 5 mg Menthol 5 mg

Purpose

Cough suppressant Oral anesthetic

Uses

temporarily relieves cough due to minor throat and bronchial irritation as may occur with the common cold occasional minor irritation, pain, sore mouth, and sore throat

Warnings

Sore throat warning if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly Do Not Use if you are now taking 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 persistent or chronic cough such as occurs with smoking, asthma, or emphysema cough that occurs with too much phlegm (mucus) Stop use and ask a doctor or dentist 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. sore mouth symptoms do not improve in 7 days irritation, pain, or redness persists or worsens 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. Sore throat warning if sore throat is...

Ask a doctor before use

persistent or chronic cough such as occurs with smoking, asthma, or emphysema cough that occurs with too much phlegm (mucus)

Stop use and ask a doctor if

Stop use and ask a doctor or dentist 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. sore mouth symptoms do not improve in 7 days irritation, pain, or redness persists or worsens

If pregnant or breast-feeding

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

adults and children 12 years of age and older: take 2 lozenges (one immediately after the other) every 4 hours as needed. Allow each lozenge to dissolve slowly in the mouth. do not take more than 12 lozenges in any 24-hour period, or as directed by a doctor children under 12 years of age: do not use

Inactive ingredients

acacia, ascorbyl palmitate, beta carotene, caramel color, corn syrup, dl-alpha tocopherol, glycerin, maltodextrin, medium-chain triglycerides, natural flavors, natural grade A honey, propylene glycol, purified water, soy lecithin, sucralose, sucrose, sunflower oil

Other information

or comments? call weekdays from 8 am to 6 pm EST at 1-800-245-1040

Label version 2, effective 19 March 2024. Retrieved from the openFDA drug label API on 4 September 2026. Read the full label on DailyMed.

Packages

The package NDC adds a third segment to the product code, identifying the pack size. See how to read an NDC.

Identical on the active ingredient

One other listing states exactly the same active ingredient at exactly the same strength in the same dosage form. They are not necessarily the same product: inactive ingredients, flavour and pack size differ, and this site does not compare prices.

Sources for this page

• FDA National Drug Code Directory entry for 0031-9306
• DailyMed label, set id 6bec225e-a203-4866-b0db-b76f73a6ae25
• How Lozenges builds these pages