Indications and uses
temporarily relieves these common cold/flu symptoms: minor aches and pains headache sore throat fever nasal congestion cough due to minor throat and bronchial irritation
Cold and Flu
- Manufacturer
- EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)
- Effective date
- 2022-09-27
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 7
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:52:48
Label at a glance#
ProductCold and Flu Daytime
Active ingredientACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE
Label structure10 sections
Dosage and administration
do not take more than directed (see overdose warning) do not take more than 4 doses in 24-hour period adults and children 12 years and over: take 2 softgels with water every 4 hours swallow whole; do not crush, chew, or dissolve children under 12 years: do not use When using Day Time and Night Time products, carefully read each label to ensure correct dosing
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredients (in each softgel)
Acetaminophen 325 mg
Dextromethoprhan HBr 10 mg
Phenlyephrine HCl 5 mg
Purposes
Pain reliever/fever reducer
Cough suppressant
Nasal decongestant
Uses
- temporarily relieves these common cold/flu symptoms:
- minor aches and pains
- headache
- sore throat
- fever
- nasal congestion
- cough due to minor throat and bronchial irritation
Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:
- more than 4,000 mg of acetaminophen I 24 hours
- with other drugs containing acetaminophen
- 3 or more alcoholic drinks everyday while using this product
Allery alert: Acetaminophen may cause severe skin reactions. Symptoms may include:
- skin reddening
- blisters
- rash
If a skin reaction occurs, stop use and seek medical help right away
Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.
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.
- with any other drug containing acetaminophen (prescription or non-prescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
Ask a doctor before use if the user has
- liver disease
- heart disease
- thyroid disease
- diabetes
- high blood pressure
- persistent or chronic cough such as occurs with smoking, asthma or emphysema
- cough that occurs with too much phlegm (mucus)
- trouble urinating due to an enlarged prostate gland
Ask a doctor or pharmacist before use if you are
taking the blood thinning drug warfarin.
When using this product,
do not exceed recommended dosage.
Stop use and ask a doctor if
- pain, cough or nasal congestion gets worse or lasts more than 7 days
- nervousness, dizziness, or sleeplessness occur
- fever gets worse or lasts more than 3 days
- redness or swelling is present
- new symptoms occur
- cough comes back or occurs, with rash or headache that lasts.
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.
Overdose warning: Taking more than the recommended dose (overdose) may cause liver damage. 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.
Directions
- do not take more than directed (see overdose warning)
- do not take more than 4 doses in 24-hour period
- adults and children 12 years and over: take 2 softgels with water every 4 hours
- swallow whole; do not crush, chew, or dissolve
- children under 12 years: do not use
- When using Day Time and Night Time products, carefully read each label to ensure correct dosing
Other information
- store between 15-30ºC (59-86º)
- avoid excessive heat
Inactive ingredients
butylated hydroxyanisole*, butylated hydroxytoluene* FD&C red #40*,FD&C yellow #6, gelatin, glycerin, polyethylene glycol, povidone, propylene glycol, purified water, sorbitan, sorbitol, titanium dioxide*, white ink
*contains one or more of these ingredients
Questions or comments?
Call 1-888-287-1915
Principal Display Panel
†Compare Vicks® DayQuil® Cold & Flu LiquiCaps® active ingredients†
DAYTIME NON-DROSWY
Cold & Flu
Multi-Symptom Relief
Acetaminophen 325 mg-Pain reliever/fever reducer
Dextromethorphan HBr 10 mg - cough suppressant
Phenylephrine HCl 5 mg - Nasal decongestant
Relieves:
- Headaches
- Fever
- Minor Aches & Pains
- Sore throat
- Cough
- Nasal Congestion
Alcohol-free Antihistamine-free
SOFTGELS**
(**Liquid-filled capsules)
TAMPER EVIDENT: DO NOT USE IF CARTON IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOW ANY SIGNS OR TAMPERING.
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.
*This product is not manufactured or distributed by The Procter & Gamble Company. Vicks® DayQuil® and LiquiCaps® are registered trademarks of The Procter & Gamble Company.
Distributed by:
Walmart Inc.,
Bentonville, AR 72716
Package Label
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 49035-542-24 | 2020-10-30 | C162847 | 48780-1 | ab0e2407-2e88-f274-e053-dbdaa90a6471 | Drug Facts |
| 49035-542-48 | 2020-10-30 | C162847 | 48780-1 | ab0e2407-2e88-f274-e053-dbdaa90a6471 | Drug Facts |
| 49035-542-24 | 2020-09-27 | C162847 | 48780-1 | ab0e2407-2e88-f274-e053-dbdaa90a6471 | Drug Facts |
| 49035-542-48 | 2020-09-27 | C162847 | 48780-1 | ab0e2407-2e88-f274-e053-dbdaa90a6471 | Drug Facts |
| 49035-542-24 | 2020-09-25 | C162847 | 48780-1 | ab0e2407-2e88-f274-e053-dbdaa90a6471 | Drug Facts |
| 49035-542-48 | 2020-09-25 | C162847 | 48780-1 | ab0e2407-2e88-f274-e053-dbdaa90a6471 | Drug Facts |
| 49035-542-24 | 2020-07-22 | C162847 | 48780-1 | ab0e2407-2e88-f274-e053-dbdaa90a6471 | Drug Facts |
| 49035-542-48 | 2020-07-22 | C162847 | 48780-1 | ab0e2407-2e88-f274-e053-dbdaa90a6471 | Drug Facts |
Products#
Every source-derived product name is available through these pages.
- Cold and Flu Daytime
- Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl
- ACETAMINOPHEN
- DEXTROMETHORPHAN HYDROBROMIDE
- DEXTROMETHORPHAN
- PHENYLEPHRINE HYDROCHLORIDE
- PHENYLEPHRINE
- BUTYLATED HYDROXYANISOLE
- FD&C YELLOW NO. 6
- GLYCERIN
- PROPYLENE GLYCOL
- WATER
- BUTYLATED HYDROXYTOLUENE
- FD&C RED NO. 40
- GELATIN
- POLYETHYLENE GLYCOL, UNSPECIFIED
- SORBITOL
- POVIDONE
- SORBITAN
- TITANIUM DIOXIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 49035-542 | 49035-542-48, 49035-542-24 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| fc0ae3ea-8ac8-4a76-b117-46286b99534f | 3b1dfc1a-1706-48e5-ae0d-9690fe3e22df | 2022-09-27 | Warnings | fc0ae3ea-8ac8-4a76-b117-46286b99534f 3b1dfc1a-1706-48e5-ae0d-9690fe3e22df |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.