TUSSIN CF- dextromethorphan hbr, guaifenesin, phenylephrine hcl liquid 
AptaPharma Inc.

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Tussin CF

Drug Facts

Active ingredients (in each 10 mL)
Dextromethorphan HBr, USP 20 mg
Guaifenesin, USP 200 mg
Phenylephrine HCl 10 mg

Purpose
Dextromethorphan HBr, USP Cough suppressant
Guaifenesin, USP Expectorant
Phenylephrine HCl 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 bronch

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 an 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 a fever • cough lasts more than 7
days, comes back, or is accompanied by fever, rash, or
persistent headache. These could be signs of aserious
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
This adult strength product is not intended for use in children under 12 years of age
mL =milliliter

Age                                                Dose
 Adults & children 12 years and over 10 mL every 4 hours
 hildren under 12 years of age Do not use

Other information
each 10 mL contains: sodium 3 mg
• store at 20-25°C (68-77°F). Do not refrigerate
• dosage cup provided

Inactive ingredients
anhydrous citric acid, flavor, purified water, sodium benzoate, sucrose

Questions? Call weekdays from 9:30 AM to 4:30 PM EST at 1-877-798-5944

Principal Display Panel

CVS
HealthTM

Compare to the active
ingredients in Robitussin® CF *

MAXIMUM STRENGTH

Non-Drowsy
Tussin CF
ADULT COUGH &
COLD

Free of alcohol, dyes &
artificial sweeteners

DEXTROMETHORPHAN HBr
Cough suppressant

GUAIFENESIN
Expectorant

PHENYLEPHRINE HCl
Nasal decongestant

Relieves:
• Cough
• Stuffy nose
• Chest congestion

For Ages
12 & Over

Cherry Flavor

8 FL OZ (237 mL)

DO NOT USE IF IMPRINTED SHRINK BAND IS MISSING OR BROKEN
Failure to follow these warnings could result in serious consequences

DO NOT REFRIGERATE. STORE AT ROOM TEMPERATURE.

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

Lot:
Exp:

LR-109 REV 01 #339103

0 50428 61580 5

DRUG FACTS →
CONTINUED
ON BACK

Distributed by: CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895
© 2018 CVS/pharmacy
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V-34690

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↓Product Package↓

311-26 Label

                                                      Tussin CF by CVS Pharmacy, Inc.

res

TUSSIN CF 
dextromethorphan hbr, guaifenesin, phenylephrine hcl liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76281-311
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) PHENYLEPHRINE10 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SUCROSE (UNII: C151H8M554)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76281-311-26237 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01208/01/201812/30/2023
Labeler - AptaPharma Inc. (790523323)
Registrant - AptaPharma Inc. (790523323)
Establishment
NameAddressID/FEIBusiness Operations
AptaPharma Inc.790523323manufacture(76281-311)

Revised: 12/2023
 
AptaPharma Inc.