Day Time Cold non drowsy cold and Flu Relief description, usages, side effects, indications, overdosage, supplying and lots more!

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Day Time Cold non drowsy cold and Flu Relief

Chain Drug Consortium, LLC (Premier Value)


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Acetaminophen 325 mg

Dextromethorphan Hydrobromide 10 mg

Phenylephrine HCl 5 mg

Pain reliever/fever reducer

Cough suppressant

Nasal decongestant

temporarily relieves common cold/ flu symptoms:

  • minor aches
  • pains
  • sore throat pain
  • fever
  • muscular aches
  • headache
  • nasal congestion
  • cough

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take

  • more than 6 doses in 24 hours, which is the maximum daily amount
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks every day while using this product

Sore throat warning: If sore throat is severe, lasts for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.

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. Quick medical attention is critical for adults and for children even if you do not notice any signs or symptoms

  • 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.
  • liver disease
  • heart disease
  • asthma
  • emphysema
  • thyroid disease
  • diabetes
  • high blood pressure
  • persistent or chronic cough
  • cough accompanied by excessive phlegm (mucus)
  • breathing problems
  • cough associated with smoking
  • trouble urinating due to an enlarged prostate gland

taking the blood thinning drug warfarin

  • do not exceed the recommended dosage
  • do not use with other products containing acetaminophen
  • do not take more than 7 days (for adults) or 5 days (for children)
  • you get nervous, dizzy or sleepless
  • fever gets worse or lasts more than 3 days
  • new symptoms occur
  • symptoms do not get better within 7 days
  • cough lasts more than 7 days (adults) or 5 days (children), comes back or occurs with rash or headache that lasts. These could be signs of a serious condition.

ask a health professional before use.

Directions

  • take every 4 hours
  • do not exceed more than 6 doses in 24 hours or as directed by a doctor. If taking DAY- TIME and NIGHT- TIME softgels limit total to 4 doses per day.
 adults and children 12 years of age and older swallow2 softgels with water
 children 4 to 12 years  ask a doctor
 children under 4 years of age  do not use
  • when using other Day time or Night time products, carefully read each label to insure correct dosing
  • store at room temperature 15o_ 30oC (59o-86oF) and avoid excessive heat
  • this product doess not contain phenylpropanolamine (PPA)
  • *This product is not manufactured or distributed by Procter & Gamble, owner of the registered trademark Vicks® DayQuil®

*butylated hydroxyanisole, *butylated hydroxytoluene, *carmine, *D&C yellow #10, FD&C red #40, FD&C yellow #6, gelatin, glycerin USP, *mannitol, polyethylene glycol 400 NF, *polyethylene glycol 600, povidone, propylene glycol USP, *sodium metabisulfite, *sorbitan, *sorbitol, sorbitol special, and white edible ink. *May also contain

Premier Value

Day- Time

Non- Drowsy Cold/ Flu Relief

Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl

Pain reliever, fever reducer, cough suppressant, nasal decongestant

*Compare to active ingredients in Vicks® DayQuil®

THIS PRODUCT IS PACKAGED IN A CHILD RESISTANT AND TAMPER EVIDENT PACKAGE. USE ONLY IF BLISTERS ARE INTACT.

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION

SEE NEW WARNINGS INFORMATION

DISTRIBUTED BY:

CHAIN DRUG CONSORTIUM, LLC.

2300 NW CORPORATE BLVD., SUITE 115

BOCA RATON, FL 33431

QUESTIONS OR COMMENTS ?

CALL TOLL FREE 1-877-753-3935

 Day Time Cold non drowsy cold and Flu Relief

DAY TIME NON DROWSY COLD/ FLU RELIEF

Day Time Cold non drowsy cold and Flu Relief

Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride CAPSULE, LIQUID FILLED

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68016-470
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ACETAMINOPHEN ACETAMINOPHEN 325 mg
DEXTROMETHORPHAN HYDROBROMIDE DEXTROMETHORPHAN 10 mg
Phenylephrine Hydrochloride PHENYLEPHRINE 5 mg

Inactive Ingredients

Ingredient Name Strength
BUTYLATED HYDROXYANISOLE
BUTYLATED HYDROXYTOLUENE
D&C YELLOW NO. 10
FD&C RED NO. 40
FD&C YELLOW NO. 6
GELATIN
GLYCERIN
mannitol
polyethylene glycol 400
POLYETHYLENE GLYCOL 600
POVIDONES
POVIDONES
propylene glycol
water
SODIUM METABISULFITE
SORBITAN
sorbitol

Product Characteristics

Color Size Imprint Code Shape
ORANGE (RED) 19 mm P19;95A;36A CAPSULE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 10 in 1 BLISTER PACK
2 NDC:68016-470-20 2 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2010-07-12


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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