Indications and uses
temporarily relieves cold symptoms cough runny nose and sneezing
temporarily relieves cold symptoms cough runny nose and sneezing
take only as recommended mL = milliliter do not exceed 4 doses per 24 hours use dosage cup provided age dose adults & children 12 years & over 30 mL every 6 hours children 4 to 11 years do not use unless directed by a doctor children under 4 years do not use When using DayTime and Nighttime products,carefully read each label to ensure correct dosing
each 30 mL contains ; sodium 36 mg store at room temperature
Dextromethorphan HBr 30 mg
Doxylamine succinate 12.5 mg
Cough suppressant
Antihistamine
temporarily relieves cold symptoms
taking sedatives or tranquilizers.
These could be signs of a serious condition.
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) immediately
| age | dose |
| adults & children 12 years & over | 30 mL every 6 hours |
| children 4 to 11 years | do not use unless directed by a doctor |
| children under 4 years | do not use |
alcohol, citric acid, FD&C blue 1, FD&C red 40, flavor, high fructose corn syrup, polyethylene glycol, propylene glycol, purified water, saccharin sodium, sodium citrate
Call 1-877-753-3935 Monday-Friday 9AM-5PM EST
COMPARE TO THE ACTIVE INGREDIENTS OF VICKS® NYQUIL® COUGH*
NIGHTTIME COUGH RELIEF
DEXTROMETHORPHAN HBr 30 mg COUGH SUPPRESSANT
DOXYLAMINE SUCCINATE 12.5 mg ANTIHISTAMINE
RELIEVES
CHERRY FLAVOR
FOR AGES 12 YEARS AND OVER
ALCOHOL 10%
ALL NIGHT COUGH RELIEF
FL OZ (mL)
*This product is not manufactured or distributed by Proctor & Gamble, owner of the registered trademark Vicks® NyQuil® Cough.
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL AROUND DOSAGE CUP OR UNDER CAP IS BROKEN OR MISSING.
Failure to follow these warnings could result in serious consequences.
PROUDLY DISTRIBUTED BY:
VALU MERCHANDISERS, CO.
5000 KANSAS AVE
KANSAS CITY, KS 66106
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 63941-345 | 63941-345-06, 63941-345-08 |
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| ff69b592-663f-4897-835f-5bf7806f6b59 | 39098716-7766-47e2-87bf-db62d710ccb8 | 2020-10-19 | Warnings | ff69b592-663f-4897-835f-5bf7806f6b59 39098716-7766-47e2-87bf-db62d710ccb8 |
Adverse event summaries are temporarily unavailable. Other product information remains available.