DAYTIME COLD AND FLU

Manufacturer
Bi-Mart | Aurohealth LLC
Effective date
2020-11-26
Label type
Human OTC Drug Label
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:03:43

Label at a glance#

ProductDAYTIME COLD AND FLU
Active ingredientACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE
Label structure16 sections

Indications and uses

temporarily relieves common cold/flu symptoms: nasal congestion cough due to minor throat & bronchial irritation sore throat headache minor aches & pains fever

Dosage and administration

take only as directed – see Overdose warning  use dose cup or tablespoon (TBSP)  do not exceed 4 doses (60 mL) (4 TBSP) per 24 hours  mL = milliliter; TBSP = tablespoon adults & children 12 years & over  30 mL (2 TBSP) every 4 hours  children 6 to under 12 years  15 mL (1 TBSP) every 4 hours  children 4 to under 6 years ask a doctor  children under 4 years do not use  when using other Daytime or Nighttime products...

Storage and handling

each 15 mL contains: sodium 49 mg store at 20° to 25°C (68° to 77°F)

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredients (in each 15 mL tablespoon)

Acetaminophen, USP 325 mg
Dextromethorphan HBr, USP 10 mg
Phenylephrine HCl, USP 5 mg

Purpose

OTC - PURPOSE SECTION

Pain reliever/fever reducer
Cough suppressant
Nasal decongestant

Uses

INDICATIONS & USAGE SECTION

temporarily relieves common cold/flu symptoms:

    • nasal congestion
    • cough due to minor throat & bronchial irritation
    • sore throat
    • headache
    • minor aches & pains
    • fever

Warnings

WARNINGS SECTION

Liver warning:


This product contains acetaminophen. Severe liver damage may occur if


  • adult takes more than 4,000 mg of acetaminophen in 24 hours

  • child takes more than 5 doses in 24 hours

  •  taken with other drugs containing acetaminophen

  •  adult has 3 or more alcoholic drinks every day while using this product


Allergy 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, lasts for more than 2 days, occurs with or is followed by fever, headache, rash, nausea, or vomiting, see a doctor promptly.

Do not use

OTC - DO NOT USE SECTION

  • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist

  •  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

OTC - ASK DOCTOR SECTION


  • liver disease

  • heart disease

  •  high blood pressure

  •  thyroid disease

  •  diabetes

  •  trouble urinating due to enlarged prostate gland

  •  cough that occurs with too much phlegm (mucus)

  •  persistent or chronic cough as occurs with smoking, asthma, or emphysema

  •  a sodium-restricted diet

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

taking the blood thinning drug warfarin

When using this product,

OTC - WHEN USING SECTION

do not use more than directed

Stop use and ask a doctor if

OTC - STOP USE SECTION


  • you get nervous, dizzy or sleepless

  •  symptoms get worse or last more than 5 days (children) or 7 days (adults)

  •  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,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Overdose warning:

Taking more than directed can cause serious health problems. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Prompt medical attention is critical for adults & for children even if you do not notice any signs or symptoms.

Directions

DOSAGE & ADMINISTRATION SECTION


  • take only as directed – see Overdose warning

  •  use dose cup or tablespoon (TBSP)

  •  do not exceed 4 doses (60 mL) (4 TBSP) per 24 hours

  •  mL = milliliter; TBSP = tablespoon


adults & children 12 years & over 
30 mL (2 TBSP) every 4 hours 
children 6 to under 12 years 
15 mL (1 TBSP) every 4 hours 
children 4 to under 6 years
ask a doctor 
children under 4 years
do not use 

  • when using other Daytime or Nighttime products, carefully read each label to ensure correct dosing


Other information

STORAGE AND HANDLING SECTION

  • each 15 mL contains: sodium 49 mg
  • store at 20° to 25°C (68° to 77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

anhydrous citric acid, carboxymethylcellulose sodium, edetate disodium, FD&C yellow no. 6, flavor, glycerin, menthol, propylene glycol, purified water, saccharin sodium, sodium benzoate, sodium chloride, sodium citrate, sorbitol, sucralose

Questions or comments?

OTC - QUESTIONS SECTION

call 1-800-935-6737
 
Distributed by:
BI-MART
Eugene, OR 97402

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL -12 FL OZ (354 mL Bottle)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BI-MART
Compare to the active ingredients
in Vicks® DayQuil® COLD & FLU
Multi-Symptom Relief*

Non-drowsy


DAYTIME
COLD & FLU
Multi-Symptom Relief

Acetaminophen USP (Pain reliever/fever reducer)
Phenylephrine HCI USP (Nasal decongestant)
Dextromethorphan HBr USP (Cough suppressant)


  • Aches, Fever & Sore Throat
  • Nasal Congestion
  • Cough 

Alcohol Free/Antihistamine Free

12 FL OZ (354 mL)



PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 12 FL OZ (354 mL Bottle)PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 12 FL OZ (354 mL Bottle)

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
37835-69537835-695-30

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
82315e79-0369-4392-ba9b-149e604ea6a7328fd31e-e715-4aa5-a0a0-ebe64f21d8d62020-11-26WarningsExact identifier
spl id: 82315e79-0369-4392-ba9b-149e604ea6a7
spl set id: 328fd31e-e715-4aa5-a0a0-ebe64f21d8d6

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.