Active ingredients (in each lozenge)

Dextromethorphan HBr 5 mg

Menthol 5 mg

Purposes

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.

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

Other information▅ store at 20°-25°C (68°-77°F)

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

Questions or comments?

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

Additional Information

PARENTS:

Learn about teen medicine abuse

www.StopMedicineAbuse.org

Keep carton for complete information.

Do not use if blister is broken or damaged.

Distributed by: Haleon, Warren, NJ 07059

Trademarks owned or licensed by Haleon.

For more recent product information, visit www.robitussin.com

Principal Display Panel

NEW! ADULT

Robitussin

Honey

MEDI-SOOTHERS

DEXTROMETHORPHAN HBr (Cough Suppressant) 5 mg

Menthol (Oral Anesthetic) 5 mg

Cough + Sore Throat

Taste the Real Honey

Relieves Cough for up to 4 HOURS
Relieves Sore Throat Pain

Honey Lemon Flavor

Actual Size

For Ages 12+

16 MEDICATED LOZENGES

202556 Front Carton

ROBITUSSIN MEDI-SOOTHERS
dextromethorphan hydrobromide, menthol lozenge

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0031-9306
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	5 mg
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	5 mg

Ingredient Name	Strength
Inactive Ingredients
ACACIA (UNII: 5C5403N26O)
ASCORBYL PALMITATE (UNII: QN83US2B0N)
BETA CAROTENE (UNII: 01YAE03M7J)
CARAMEL (UNII: T9D99G2B1R)
CORN SYRUP (UNII: 9G5L16BK6N)
.ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)
GLYCERIN (UNII: PDC6A3C0OX)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
HONEY (UNII: Y9H1V576FH)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
SUCRALOSE (UNII: 96K6UQ3ZD4)
SUCROSE (UNII: C151H8M554)
SUNFLOWER OIL (UNII: 3W1JG795YI)

Product Characteristics
Color	yellow	Score	no score
Shape	OVAL	Size	25mm
Flavor	HONEY (Honey Lemon)	Imprint Code	R
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:0031-9306-01	8 in 1 BLISTER PACK; Type 0: Not a Combination Product	06/01/2023
2	NDC:0031-9306-02	16 in 1 BLISTER PACK; Type 0: Not a Combination Product	06/01/2023

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M012	06/01/2023

Labeler - Haleon US Holdings LLC (079944263)

Drug Facts