TUSSIN CF- dextromethorphan hbr, guaifenesin, phenylephrine hcl liquid

Tussin CF by

Drug Labeling and Warnings

Tussin CF by is a Otc medication manufactured, distributed, or labeled by AptaPharma Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

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

PURPOSE

Purpose
Dextromethorphan HBr, USP Cough suppressant
Guaifenesin, USP Expectorant
Phenylephrine HCl Nasal Decongestant

INDICATIONS & USAGE

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

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 DOCTOR

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 DOCTOR/PHARMACIST

Ask a doctor or pharmacist before use if you are taking any
other oral nasal decongestant or stimulant

WHEN USING

When using this product do not use more than directed

STOP USE

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.

PREGNANCY 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.

DOSAGE & ADMINISTRATION

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

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

OTHER SAFETY INFORMATION

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

INACTIVE INGREDIENT

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

QUESTIONS

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
CVS.com® 1-800-SHOP CVS

V-34690

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↓Product Package↓

                                                      Tussin CF by CVS Pharmacy, Inc.

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INGREDIENTS AND APPEARANCE

TUSSIN CF 
dextromethorphan hbr, guaifenesin, phenylephrine hcl liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76281-311
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	20 mg  in 10 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	200 mg  in 10 mL
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV)	PHENYLEPHRINE	10 mg  in 10 mL

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SUCROSE (UNII: C151H8M554)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76281-311-26	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	08/01/2018

Labeler - AptaPharma Inc. (790523323)

Registrant - AptaPharma Inc. (790523323)

Establishment
Name	Address	ID/FEI	Business Operations
AptaPharma Inc.		790523323	manufacture(76281-311)