Label: KROGER NITETIME COLD AND FLU- choline salicylate, diphenhydramine hydrochloride, phenylephrine hydrochloride liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

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.

Drug Label Information

Updated June 30, 2016

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredients

    (in each 30 mL (2 TBSP))

    Choline Salicylate (NSAID)* 870 mg

    Diphenhydramine HCl 50 mg

    Phenylephrine HCl 10 mg

    *nonsteroidal anti-inflammatory drug

  • PURPOSE

    Purpose

    Pain reliever / fever reducer

    Antihistamine

    Nasal decongestant

  • INDICATIONS & USAGE

    Uses

    Temporarily relieves these common cold and flu symptoms:

    • nasal congestion
    • minor aches and pains
    • sore throat
    • headache
    • runny nose
    • sneezing
    • watery eyes
    • temporarily reduces fever
  • WARNINGS

    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 warning:

    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

    Do not use

    • if you have ever had an allergic reaction to salicylates (including aspirin) or any other pain reliever / fever reducer.
    • with any other drug containing diphenhydramine, even one used on the skin
    • 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.
    • in children under 12 years of age
  • ASK DOCTOR

    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, thyroid disease, or glaucoma
    • you have a cough with excessive phlegm (mucus)
    • you have difficulty in urination due to enlargement of the prostate gland
    • you have breathing problems such as emphysema or chronic bronchitis
    • you have persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema
    • you have a sodium restricted diet.
  • ASK DOCTOR/PHARMACIST

    Ask a doctor or pharmacist before use if you are

    • taking a precription drug for anti-coagulation (thinning the blood), diabetes, gout, or arthritis
    • taking a diuretic
    • under a doctor's care for any serious condition
    • taking sedatives or tranquilizers
  • WHEN USING

    When using this product

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

    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
  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast-feeding, ask a health professional before use. It is especially important not to use salicylates (NSAIDs) 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

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

  • DOSAGE & ADMINISTRATION

    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
    • TBSP=tablespoon
    • mL-milliliter
    • Adults and children 12 years and over: 30 mL (2 TBSP) every 4 hours
    • Children under 12: Do not use
  • STORAGE AND HANDLING

    Other information

    • each 30 mL (2 TBSP) contains: Sodium 25 mg
    • tamper evident: Do not use if foil seal under cap is broken or missing.
    • read all product information before using
    • store at room temperature 68°-86°F (20°-30°C)
    • avoid excessive heat and humidity
  • INACTIVE INGREDIENT

    Inactive ingredients

    Edetate disodium, glycerin, propylene glycol, purified water, sodium citrate, sodium saccharin, sorbitol.

  • QUESTIONS

    Questions or comments?

    1-800-632-6900

  • Kroger NiteTime Cold & Flu 8 fl oz (237 mL) Bottle Label

    Kroger NiteTime Label1

    Kroger NiteTime Label2

  • INGREDIENTS AND APPEARANCE
    KROGER NITETIME COLD AND FLU 
    choline salicylate, diphenhydramine hydrochloride, phenylephrine hydrochloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-772
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE50 mg  in 30 mL
    CHOLINE SALICYLATE (UNII: KD510K1IQW) (SALICYLIC ACID - UNII:O414PZ4LPZ) CHOLINE SALICYLATE870 mg  in 30 mL
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE10 mg  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SORBITOL (UNII: 506T60A25R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:30142-772-08237 mL in 1 BOTTLE; Type 0: Not a Combination Product04/07/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34104/07/2016
    Labeler - THE KROGER CO (006999528)