TUSSIN CF- robitussin cf liquid 
Select Brand Dist.

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.

----------

Drug Facts

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

Select brand

COUGH CONTROL

COUGH SUPPRESSANT (DEXTROMETHORPHAN HBr)

EXPECTORANT (Guaifenesin)

NASAL DECONGESTANT (Phenylephrine HCl)

CONTROLS COUGHS

LOOSENS AND RELIEVES CHEST CONGESTION

HELPS CLEAR NASAL PASSAGES

ALCOHOL-FREE

FOR ADULTS

COMPARE TO ACTIVE INGREDIENTS OF ROBITUSSIN CF

SEE NEW DOSING INFORMATION

4 FL OZ (118ML)

IMAGE OF LABEL


TUSSIN CF 
robitussin cf liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:15127-943
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 5 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN100 mg  in 5 mL
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
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)  
Product Characteristics
ColorRED (Red 40) Score    
ShapeSize
FlavorCHERRY (cherry) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:15127-943-04118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/21/200905/01/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34108/21/200905/01/2017
Labeler - Select Brand Dist. (012578514)

Revised: 6/2017
 
Select Brand Dist.