TUSSIN CF- robitussin cf liquid

Tussin CF by

Drug Labeling and Warnings

Tussin CF by is a Otc medication manufactured, distributed, or labeled by Rite Aid Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Dextromethorphan HBr, USP 10 mg
Guaifenesin, USP 100 mg
Phenylephrine HCI, USP 5 mg

Purpose

Cough suppressant
Expectorant
Nasal decongestant

Uses

helps loosen phlegm (mucus) and thin bronchial
secretions to drain bronchial tubes

temporarily relieves cough due to minor throat
and bronchial irritation as may occur 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 diabetes
high blood pressure thyroid disease
cough that lasts or is chronic such as occurs with
smoking, asthma, chronic bronchitis or emphysema
cough that occurs with too much phlegm (mucus)
trouble urinating due to an enlarged prostate gland

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 this and all drugs out of the reach of children.

In case of accidental overdose, seek professional
assistance or contact a Poison Control Center
immediately.

Directions

do not exceed 6 doses in a 24-hour period
this adult product is not intended for use in
children under 12 years of age

adults and children 12 years and over      2 teaspoonfuls (tsps) every 4 hours

children under 12 years                          do not use

Other information

  alcohol-free dosage cup provided
store at controlled room temperature

Inactive ingredients

citric acid, flavor, glycerin,
lactic acid, menthol, propylene glycol, purified water,
red 40, sodium benzoate, sorbitol, sucralose

Principal Display Panel

Rite Aid Pharmacy

Compare to the Active Ingredients in Robitussin CF

tussin cough and cold CF

Dextromethorphan HBr, 10 mg

guaifenesin, 100 mg

Phenylephrine HCI, 5 mg

cough suppressant, expectorant

and nasal decongestant

Non-Drowsy

Alcohol Free

Relieves- coughs, stuffy nose, chest congestion and mucus

12 years and older

4 FL Oz (118 mL)

INGREDIENTS AND APPEARANCE

TUSSIN CF 
robitussin cf liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11822-0126
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	10 mg  in 5 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	100 mg  in 5 mL
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV)	PHENYLEPHRINE HYDROCHLORIDE	5 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
LACTIC ACID (UNII: 33X04XA5AT)
MENTHOL (UNII: L7T10EIP3A)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SORBITOL (UNII: 506T60A25R)
SUCRALOSE (UNII: 96K6UQ3ZD4)
FD&C RED NO. 40 (UNII: WZB9127XOA)

Product Characteristics
Color		Score
Shape		Size
Flavor	CHERRY (cherry)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11822-0126-4	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/13/2013	12/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part341	11/13/2013	12/30/2020

Labeler - Rite Aid Corporation (014578892)