DAYCLEAR SINUS PAIN AND PRESSURE- choline salicylate, guaifenesin, phenylephrine hydrochloride liquid 
GM Pharmaceuticals, INC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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DAYCLEAR SINUS PAIN AND PRESSURE

DAYCLEAR SINUS PAIN AND PRESSURE- choline salicylate, guaifenesin, phenylephrine hydrochloride liquid

GM Pharmaceuticals, Inc.

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DayClear Sinus Pain & Pressure

Drug Facts:

Active ingredients (in each 30 mL)


Choline Salicylate (NSAID)* 870 mg

Guaifenesin 200 mg

Phenylephrine HCl 10 mg

Purpose

Pain reliever/fever reducer

Expectorant

Nasal decongestant

*nonsteroidal anti-inflammatory drug

Uses

temporarily relieves nasal congestion due to common cold, hay fever, and other upper respiratory allergies

▪ nasal congestion

▪ minor aches and pains

▪ headache

▪ temporarily reduces fever

▪ sore throat

▪ helps loosen phlegm (mucus) and thin bronchial secretions to rid bronchial passageways of bothersome mucus and make coughs more productive

Warnings

Reye's syndrome

Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye's syndrome, a rare but serious illness.

Allergy alert

Salicylates (NSAIDs) may cause a severe allergic reaction which may include:

▪ hives

▪ rash

▪ shock

▪ skin reddening

▪ facial swelling

▪ asthma (wheezing)

Stomach bleeding warnings

This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you:

▪ are age 60 or older

▪ have had stomach ulcers or bleeding problems

▪ take a blood thinning (anticoagulant) or steroid drug

▪ take other drugs containing prescription or non-prescription NSAIDs (aspirin, ibuprofen, naproxen, or others)

▪ have 3 or more alcoholic drinks every day while using this product

▪ take more or for a longer time than directed

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 have ever had an allergic reaction to salicylates (including aspirin) or any other pain reliever/ fever reducer.

▪ if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or 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.

▪ if you have ever had an allergic reaction to this product or any of its ingredients

▪ in children under 12 years of age

Ask a doctor before use if

▪ stomach bleeding warning applies to you

▪ you have a history of stomach problems, such as heartburn or if you have ulcers or bleeding problems

▪ you have high blood pressure, heart disease, liver cirrhosis, kidney disease, diabetes or thyroid disease

▪ you have a cough with excessive phlegm (mucus)

▪ you have difficulty in urination due to enlargement of the prostate gland

▪ you have a persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema

▪ you have asthma

Ask a doctor or pharmacist before use if you are

▪ taking a prescription drug for anticoagulation (thinning the blood), diabetes, gout, or arthritis.

▪ under a doctor’s care for any serious condition

▪you are taking a diuretic

When using this product do not exceed recommended dosage

Stop use and ask a doctor if

▪ an allergic reaction occurs. Seek medical help right away.

▪ 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

▪ ringing in the ears or a loss of hearing occurs

▪ cough comes back or occurs with rash or headache that lasts. These could be signs of a serious condition.

▪ nervousness, dizziness, or sleeplessness occurs

▪ you experience any of the following signs of stomach bleeding:

▪ feel faint

▪ vomit blood

▪ have bloody or black stools

▪ have stomach pain that does not get better

If pregnant or breast-feeding,

ask a health professional before use. It is especially important not to use salicylates (NSAID) during the last 3 months of pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

  • do not exceed recommended dosage.
  • do not take more than 6 doses in any 24-hour period.
  • use enclosed dose cup
  • keep dosage cup with product
  • mL = milliliters
  • adults and children 12 years of age and over: 30mL every 4 hours
  • children under 12 years of age: do not use

Other information

  • each 30mL contains: Sodium 12 mg
  • tamper evident: Do not use if foil seal under cap is broken or missing.
  • read all product information before using
  • store at 68° to 86°F (20° to 30°C)
  • avoid excessive heat and humidity

Inactive ingredients

anhydrous citric acid, glycerin, propylene glycol, purified water, sodium benzoate, sodium citrate, sodium saccharin, sorbitol

Questions or Comments?

Call 1-888-535-0305 9a.m.- 5p.m. CST

R062716M

PRINCIPAL DISPLAY PANEL

NDC 58809-312-08
DayClear
SINUS
PAIN & PRESSURE
8 fl oz (237 mL)

PRINCIPAL DISPLAY PANEL
NDC 58809-312-08
DayClear
SINUS
PAIN & PRESSURE
8 fl oz (237 mL)

PRINCIPAL DISPLAY PANEL
NDC 58809-312-08
DayClear
SINUS
PAIN & PRESSURE
8 fl oz (237 mL)

PRINCIPAL DISPLAY PANEL
NDC 58809-312-08
DayClear
SINUS
PAIN & PRESSURE
8 fl oz (237 mL)

DAYCLEAR SINUS PAIN AND PRESSURE 
choline salicylate, guaifenesin, phenylephrine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58809-312
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN200 mg  in 30 mL
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE10 mg  in 30 mL
CHOLINE SALICYLATE (UNII: KD510K1IQW) (SALICYLIC ACID - UNII:O414PZ4LPZ) CHOLINE SALICYLATE870 mg  in 30 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SORBITOL (UNII: 506T60A25R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58809-312-08237 mL in 1 BOTTLE; Type 0: Not a Combination Product08/10/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34108/10/201512/10/2018
Labeler - GM Pharmaceuticals, INC (793000860)

Revised: 11/2019
 
GM Pharmaceuticals, INC