Safeway Daytime Cold and Flu Relief description, usages, side effects, indications, overdosage, supplying and lots more!

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Safeway Daytime Cold and Flu Relief

Safeway

Safeway Daytime Cold and Flu Relief


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients (in each softgel)

Acetaminophen 325mg USP

Dextromethoprhan Hydrobromide 10mg

Phenlyephrine HCl 5mg


Purpose

Pain reliever/Fever reducer

Cough suppressant

Nasal decongestant

Safeway Daytime Cold and Flu Relief Uses

temporarily relieves common cold/flu symptoms:

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

Warnings

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 more alcoholic drinks everyday while using this product.
Sore throat warning:



Do not use

with other drugs containing acetaminophen (prescription or non prescription). 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

  • Liver disease
  • heart disease
  • thyroid disease
  • diabetes
  • high blood pressure
  • trouble urinating due to an enlarged prostate gland
  • persistent or chronic cough as occurs with smoking, asthma, or emphysema

Ask a doctor or pharmacist before use if you are

taking the blood thinning drug warfarin

When using this product


Stop use and ask a doctor if

  • 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

ask a health care professional before use.

Keep out of reach of children.

Overdose warning: Taking more than the recommended dose (overdose) could cause serious health problems. In case of overdose. get medical help or contact a Poison Control Center right away: 1800-222-1222. Prompt medical attention is critical for adults as well as children even if you do not notice any signs or symptoms.

Directions

  • take only as directed - see Overdose warning
  • do not exceed 4 doses per 24 hours

adults and children 12 years and older
swallow 2 softgels with water every 4 hours
children 4 to under 12 years
ask a doctor
children under 4 years
do not use

  • when using other Day Time or Night Time products, carefully read each label to insure correct dosing.

Safeway Daytime Cold and Flu Relief Other information

  • store at room temperature 15 to 30 degrees C (59-86degrees F) and avoid excessive heat
  • this product does not contain phelylpropanolamine (PPA)
  • *This product is not manufactured or distributed by Procter and Gamble, owner of the registered trademark Vicks(r) DayQuil(r)

Questions or comments?

Call 1-888-SAFEWAY Monday - Friday 7AM - 6PM PST

*This product is not manufactured or distributed by Procter and Gamble, owner of the registered trademark Vicks Dayquil Liquicaps

Inactive Ingredients

butylated hydroxyanisole, butylated hydroxytoluene*, edible white printing ink, FDandC Red No. 40*, FDandC yellow No. 6, gelatin, glycerin, polyethylene glycol, povidone, propylene glycol, purified water, sorbitan, sorbitol.

*may contain this ingredient

Product Labeling

Safeway Daytime Cold and Flu Relief

Safeway Daytime Cold and Flu Relief

ACETAMINOHPEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCL CAPSULE, LIQUID FILLED

Product Information

Product Type Human otc drug label Item Code (Source) NDC:21130-470
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
FD&C YELLOW NO. 6
GELATIN
GLYCERIN
POLYETHYLENE GLYCOL 600
povidone
propylene glycol
water
SORBITAN
sorbitol

Product Characteristics

Color Size Imprint Code Shape
orange (Orange) 20 mm 36A;95A;P19 CAPSULE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 24 in 1 BLISTER PACK
2 NDC:21130-470-24 2 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2012-11-08


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