TUSSIN CF - dextromethorphan hbr guaifenesin phenylephrine hcl solution 
Strategic Sourcing Services

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Tussin CF
Dextromethorphan HBr Guaifenesin Phenylephrine HCl

Active ingredients (in each 10 mL)


Dextromethorphan HBrDextromethorphan HBr, USP 20 mg
Guaifenesin, USP 200 mg
Phenylephrine HCI, USP 10 mg

Purposes

Cough suppressant
Expectorant
Nasal decongestant

Uses


■ helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes
■ temporarily relieves these symptoms occurring with a cold:
  • nasal congestion
  • cough due to minor throat and bronchial irritation.

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


■ heart disease          ■ high blood pressure
■ thyroid disease        ■ diabetes
■ trouble urinating due to enlarged prostate gland
■ cough that occurs with too much phlegm (mucus)
■ cough that lasts or is chronic such as occurs with smoking,asthma, chronic bronchitis or emphysema.

Ask a doctor or pharmacist before use if you are


taking any other oral nasal decongestant or stimulant.


When using this product do not use more than directed.

Stop use and ask a doctor if


■ you get nervous, dizzy or sleepless
■ symptoms do not get better within 7 days or are accompanied by fever
■ 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 (1-800-222-1222).

Directions


■ mL = milliliter
■ do not take more than 6 doses in any 24 hour period
■ this adult strength product is not intended for use in children under 12 years of age
■ measure only with dosing cup provided
■ keep dosing cup with product


AGE
DOSE
Adults and children 12 years and over
10 mL every 4 hours
Children under 12 years
do not use

Other information


■ each 10 mL contains: sodium 6 mg
■ store at 20-25°C (68-77°F)       ■ do not refrigerate
■ Keep carton for full Direction for use

Inactive ingredients


anhydrous citric acid, FD&C red no.40, glycerin, menthol, natural & artificial flavor, propylene glycol,purified water, sodium benzoate, sorbitol solution, sucralose

Questions or comments?


Call 833-358-6431Monday to Friday 9:00am to 7:00pm EST

©2023 McKesson Corporation
Distributed by:McKesson Corp., via Strategic Sourcing Services LLC.
Memphis, TN 38141
Money Back Guarantee
www.fosterandthrive.com

*This product is not manufactured or distributed by Pfizer,
owner of the registered trademark Robitussin ®

PRINCIPAL DISPLAY PANEL

Dextromethorphan HBr Guaifenesin Phenylephrone HCL-237 mL

Dextromethorphan HBr Guaifenesin Phenylephrone HCL-237 mL

TUSSIN CF  
dextromethorphan hbr guaifenesin phenylephrine hcl solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70677-1187
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
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE10 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
MENTHOL (UNII: L7T10EIP3A)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SORBITOL SOLUTION (UNII: 8KW3E207O2)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70677-1187-11 in 1 CARTON08/09/2023
1237 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34108/09/2023
Labeler - Strategic Sourcing Services (116956644)
Establishment
NameAddressID/FEIBusiness Operations
AptaPharma Inc.790523323manufacture(70677-1187)

Revised: 8/2023
Document Id: 031de007-e388-59fe-e063-6294a90a14b8
Set id: e416982f-6cbb-4f48-a215-16bea8393dad
Version: 1
Effective Time: 20230817
 
Strategic Sourcing Services