Cold And Flu
FDA Label NDC 41250-762

19 label sections · Submitted to the FDA by Meijer Distribution, Inc · Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Meijer Distribution, Inc for the product Cold And Flu (NDC 41250-762). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredients (in each liquid-filled capsule) (daytime cold & flu), purpose, active ingredients (in each liquid-filled capsule) (nighttime cold & flu), uses, warnings, do not use, ask a doctor before use if you have, ask a doctor or pharmacist before use if you are, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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Compare to Vicks® DayQuil® &

NyQuil® Cold & Flu LiquiCaps®

active ingredients†

DAYTIME • NON DROWSY

Cold & Flu

ACETAMINOPHEN /

PAIN RELIEVER / FEVER REDUCER

DEXTROMETHORPHAN HBr /

COUGH SUPPRESSANT

PHENYLEPHRINE HCl /

NASAL DECONGESTANT

MULTI-SYMPTOM

ACTUAL

SIZE

32

LIQUID

CAPS

NIGHTTIME

Cold & Flu

ACETAMINOPHEN /

PAIN RELIEVER / FEVER REDUCER

DEXTROMETHORPHAN HBr /

COUGH SUPPRESSANT

DOXYLAMINE SUCCINATE /

ANTIHISTAMINE

MULTI-SYMPTOM

ACTUAL

SIZE

16

LIQUID

CAPS

48 TOTAL LIQUID CAPS

TAMPER EVIDENT: DO NOT USE IF PACKAGE IS OPENED

OR IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY

SIGNS OF TAMPERING

††This product is not manufactured or

distributed by Procter & Gamble, owner of the

registered trademark Vicks® DayQuil® &

NyQuil® Cold & Flu LiquiCaps®.

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* Please review the disclaimer below.