VICKS NYQUIL COLD AND FLU NIGHTTIME RELIEF
-
acetaminophen,
dextromethorphan hydrobromide and
doxylamine succinate liquid
Procter & Gamble Manufacturing Company
----------
VICKS®Drug Facts
| Active ingredients (in each 15 ml tablespoon) | Purpose |
|---|---|
| Acetaminophen 500 mg | Pain reliever/fever reducer |
| Dextromethorphan HBr 15 mg | Cough suppressant |
| Doxylamine succinate 6.25 mg | Antihistamine |
temporarily relieves common cold/flu symptoms:
This product contains acetaminophen. Severe liver damage may occur if you take:
If sore throat is severe, persists for more than two days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.
Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers.
These could be signs of a serious condition.
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children.
Taking more than the recommended dose can cause serious health problems. In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.
| adults and children 12 years and over | 30 ml (2 TBSP) every 6 hours |
| children 4 to under 12 years | ask a doctor |
| children under 4 years | do not use |
alcohol, citric acid, D&C Yellow No. 10, FD&C Green No. 3, FD&C Yellow No. 6, flavor, high fructose corn syrup, polyethylene glycol, propylene glycol, purified water, saccharin sodium, sodium citrate
1-800-362-1683
Dist. by Procter & Gamble,
Cincinnati OH 45202.
www.vicks.com
BONUS
20% MORE
than the 10oz size
VICKS®
NyQuil®
Original
Flavor
COLD & FLU
Multi-Symptom Relief
Acetaminophen…Aches, Fever
Dextromethorphan…Cough
Doxylamine…Sneezing, Runny Nose
Alcohol 10%
12 FL OZ (354 ml)
See Drug Facts

| VICKS NYQUIL
COLD AND FLU NIGHTTIME RELIEF
acetaminophen, dextromethorphan hydrobromide, and doxylamine succinate liquid |
|||||||||||||||||||||
|
|||||||||||||||||||||
|
|||||||||||||||||||||
|
|||||||||||||||||||||
|
|||||||||||||||||||||
|
|||||||||||||||||||||
| Marketing Information | |||
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| OTC monograph final | part341 | 04/20/2009 | 06/01/2009 |
| Labeler - Procter & Gamble Manufacturing Company (004238200) |