smart sense sinus relief

Manufacturer
Kmart Corporation
Effective date
2019-12-11
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:52:48

Label at a glance#

Productsmart sense sinus relief
Active ingredientACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, DIPHENHYDRAMINE HYDROCHLORIDE
Label structure19 sections

Indications and uses

• temporarily relieves: • nasal congestion • headache • minor aches and pains • sinus congestion and pressure • runny nose and sneezing (SINUS RELIEF Night only) • temporarily promotes nasal and/or sinus drainage • helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive (SINUS RELIEF Day only)

Dosage and administration

• do not take more than directed (see Overdose warning) • do not take more than 10 caplets in any 24-hour period • adults and children 12 years of age and older: take 2 caplets every 4 hours • children under 12 years of age: do not use

Storage and handling

• each caplet contains: sodium 4 mg (SINUS RELIEF Day only) • store at 20-25 ° C (68-77 ° F)

Label contents#

Full prescribing information#

Active ingredients (in each caplet) – SINUS RELIEF Day

OTC - ACTIVE INGREDIENT SECTION

Acetaminophen 325 mg

Guaifenesin 200 mg

Phenylephrine HCl 5 mg

Active ingredients (in each caplet) – SINUS RELIEF Night

OTC - ACTIVE INGREDIENT SECTION

Acetaminophen 325 mg

Diphenhydramine HCl 25 mg

Phenylephrine HCl 5 mg

Purposes – SINUS RELIEF Day

OTC - PURPOSE SECTION

Pain reliever

Expectorant

Nasal decongestant

Purposes – SINUS RELIEF Night

OTC - PURPOSE SECTION

Pain reliever

Antihistamine

Nasal decongestant

Uses

INDICATIONS & USAGE SECTION

  • temporarily relieves:
  • nasal congestion
  • headache
  • minor aches and pains
  • sinus congestion and pressure
  • runny nose and sneezing (SINUS RELIEF Night only)
  • temporarily promotes nasal and/or sinus drainage
  • helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive (SINUS RELIEF Day only)

Warnings

WARNINGS SECTION

Liver warning: These products contain acetaminophen. Severe liver damage may occur if you take

  • more than 4,000 mg of acetaminophen in 24 hours
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks every day while using these products

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.

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.
  • with any other product containing diphenhydramine, even one used on skin (SINUS RELIEF Night only)
  • 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 these products.
  • if you have ever had an allergic reaction to these products or any of their ingredients

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • liver disease
  • heart disease
  • diabetes
  • high blood pressure
  • thyroid disease
  • trouble urinating due to an enlarged prostate gland
  • glaucoma (SINUS RELIEF Night only)
  • a breathing problem such as emphysema or chronic bronchitis (SINUS RELIEF Night only)
  • persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema (SINUS RELIEF Day only)
  • cough that occurs with too much phlegm (mucus) (SINUS RELIEF Day only)

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

  • taking the blood thinning drug warfarin
  • taking sedatives or tranquilizers (SINUS RELIEF Night only)

When using these products

OTC - WHEN USING SECTION

  • do not use more than directed
  • excitability may occur, especially in children (SINUS RELIEF Night only)
  • marked drowsiness may occur (SINUS RELIEF Night only)
  • alcohol, sedatives, and tranquilizers may increase drowsiness (SINUS RELIEF Night only)
  • avoid alcoholic drinks (SINUS RELIEF Night only)
  • be careful when driving a motor vehicle or operating machinery (SINUS RELIEF Night only)

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • nervousness, dizziness, or sleeplessness occur
  • pain, cough or nasal congestion gets worse or lasts more than 7 days
  • 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 persistent headache. These could be signs of a serious condition. (SINUS RELIEF Day only)

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: In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

DOSAGE & ADMINISTRATION SECTION

  • do not take more than directed (see Overdose warning)
  • do not take more than 10 caplets in any 24-hour period
  • adults and children 12 years of age and older: take 2 caplets every 4 hours
  • children under 12 years of age: do not use

Other information

STORAGE AND HANDLING SECTION

  • each caplet contains: sodium 4 mg (SINUS RELIEF Day only)
  • store at 20-25°C (68-77°F)

Inactive ingredients - SINUS RELIEF Day only

INACTIVE INGREDIENT SECTION

croscarmellose sodium, crospovidone, FD&C yellow #6 aluminum lake, maltodextrin, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone, pregelatinized starch, silicon dioxide, stearic acid, talc, titanium dioxide

Inactive ingredients - SINUS RELIEF Night only

INACTIVE INGREDIENT SECTION

crospovidone, FD&C blue #1 aluminum lake, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone, pregelatinized starch, silicon dioxide, stearic acid, talc, titanium dioxide

Questions or comments?

OTC - QUESTIONS SECTION

1-800-719-9260

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SEE NEW WARNINGS

COMPARE TO ACTIVE INGREDIENTS IN MUCINEX® SINUS-MAX®

ACTUAL SIZE

daytime

sinus relief

ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCl

PAIN RELIEVER, EXPECTORANT, NASAL DECONGESTANT

MAXIMUM STRENGTH

10 CAPLETS

RELIEVES:

SINUS PRESSURE

HEADACHE – CONGESTION

THINS & LOOSENS MUCUS

nighttime

sinus relief

ACETAMINOPHEN, DIPHENHYDRAMINE HCl, PHENYLEPHRINE HCl

PAIN RELIEVER, ANTIHISTAMINE, NASAL DECONGESTANT

MAXIMUM STRENGTH

RELIEVES:

NASAL CONGESTION

SINUS PRESSURE & PAIN

RUNNY NOSE – SNEEZING

10 CAPLETS

Smart Sense Sinus Relief Image 1
Smart Sense Sinus Relief Image 1
Smart Sense Sinus Relief Image 2
Smart Sense Sinus Relief Image 2

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49738-93649738-936-80

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 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
6c26d6c3-c06f-4f87-bf1b-026f2327ef154e472e39-a5ea-4e65-bcb9-6cc6ecf0b2322021-10-05WarningsExact identifier
spl set id: 4e472e39-a5ea-4e65-bcb9-6cc6ecf0b232

Reported adverse events (FAERS/openFDA)#

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