Tussin CF
- Manufacturer
- AptaPharma Inc.
- Effective date
- 2019-12-09
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 23:52:42
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
OTC - ACTIVE INGREDIENT SECTION
Active ingredients (in each 10 mL)
Dextromethorphan HBr, USP 20 mg
Guaifenesin, USP 200 mg
Phenylephrine HCl 10 mg
OTC - PURPOSE SECTION
Purpose
Dextromethorphan HBr, USP Cough suppressant
Guaifenesin, USP Expectorant
Phenylephrine HCl Nasal Decongestant
INDICATIONS & USAGE SECTION
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 SECTION
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.
OTC - ASK DOCTOR SECTION
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
OTC - ASK DOCTOR/PHARMACIST SECTION
Ask a doctor or pharmacist before use if you are taking any
other oral nasal decongestant or stimulant
OTC - WHEN USING SECTION
When using this product do not use more than directed
OTC - STOP USE SECTION
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.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding, ask a health professional
before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. In case of overdose, get
medical help or contact a Poison Control Center right
away.
DOSAGE & ADMINISTRATION SECTION
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 SECTION
Inactive ingredients
anhydrous citric acid, flavor, purified water, sodium benzoate, sucrose
OTC - QUESTIONS SECTION
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
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V-34690
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↓Product Package↓
Tussin CF by CVS Pharmacy, Inc.
res
Products#
Every source-derived product name is available through these pages.
- Tussin CF
- DEXTROMETHORPHAN HBr, GUAIFENESIN, PHENYLEPHRINE HCl
- DEXTROMETHORPHAN HYDROBROMIDE
- DEXTROMETHORPHAN
- GUAIFENESIN
- PHENYLEPHRINE HYDROCHLORIDE
- PHENYLEPHRINE
- ANHYDROUS CITRIC ACID
- WATER
- SODIUM BENZOATE
- SUCROSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 76281-311 | 76281-311-26 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| DEXTROMETHORPHAN HYDROBROMIDE | 9D2RTI9KYH | ACTIB |
| GUAIFENESIN | 495W7451VQ | ACTIB |
| PHENYLEPHRINE HYDROCHLORIDE | 04JA59TNSJ | ACTIM |
| ANHYDROUS CITRIC ACID | XF417D3PSL | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM BENZOATE | OJ245FE5EU | IACT |
| SUCROSE | C151H8M554 | IACT |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 4167c0ba-3fa3-421f-b742-a06b9f5b9e45 | 0da76857-71ab-433d-9ad9-415ed94ce5ff | 2023-12-30 | Warnings | 0da76857-71ab-433d-9ad9-415ed94ce5ff |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
