TUSSIN DM COUGH AND CHEST CONGESTION ADULT- dextromethorphan hbr, guaifenesin liquid 
P & L Development, LLC

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Drug Facts

Active ingredients (in each 10 mL)

Dextromethorphan HBr 20 mg

Guaifenesin 200 mg

Purposes

Cough suppressant

Expectorant

Uses

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 (1-800-222-1222) right away.

Directions

Other information

Inactive ingredients

citric acid, FD&C red# 40, flavor, glucose, glycerin, high fructose corn syrup, menthol, purified water, saccharin sodium, sodium benzoate

Questions or comments?

Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

Principal Display Panel

Compare to the active ingredients in Robitussin® Cough + Chest Congestion DM*

adult tussin cough + chest congestion DM

Dextromethorphan HBr 20 mg

Guaifenesin 200 mg

cough suppressant

expectorant

relieves:

for ages 12+

alcohol free

non-drowsy

fl oz (mL)

*This product is not manufactured or distributed by Haleon group of companies, distributor of Robitussin® Cough+Chest Congestion DM.

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL AROUND BOTTLE OR UNDER CAP IS BROKEN OR MISSING.

Manufactured by:

PL Developments

 11865 S. Alameda St

Lynwood, CA 90262

Package Label

Dextromethorphan HBr 20 mg Guaifenesin 200 mg

Readyincase - Adult Tussin cough & chest congestion DM

TUSSIN DM COUGH AND CHEST CONGESTION  ADULT
dextromethorphan hbr, guaifenesin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49580-0385
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 mg  in 10 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN200 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
DEXTROSE (UNII: IY9XDZ35W2)  
GLYCERIN (UNII: PDC6A3C0OX)  
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
MENTHOL (UNII: L7T10EIP3A)  
WATER (UNII: 059QF0KO0R)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49580-0385-41 in 1 BOX03/31/2015
1118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2NDC:49580-0385-2118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/31/2015
3NDC:49580-0385-81 in 1 BOX03/31/2015
3237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01203/31/2015
Labeler - P & L Development, LLC (101896231)

Revised: 1/2024
Document Id: 3e460b8c-7feb-4630-a992-ea374a60a7eb
Set id: 4af67ba7-8892-442c-b9fb-80aba9140e05
Version: 11
Effective Time: 20240126
 
P & L Development, LLC