Daytime Severe Cold And Flu Relief Softgels
FDA Label NDC 36800-655

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Topco Associates Llc for the product Daytime Severe Cold And Flu Relief Softgels (NDC 36800-655). 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 softgel), purpose, uses, warnings, do not use, ask a doctor before use if you have, ask a doctor or pharmacist before use if you are, when using this product,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Principal Display Panel

Compare to the active ingredients in Vicks® DayQuil® Cold & Flu*

MAXIMUM STRENGTH

Daytime Softgels

Severe Cold/Flu Relief

ACETAMINOPHEN - Pain reliever; fever reducer

DEXTROMETHORPHAN HBr - Cough Suppressant

GUAIFENESIN- Expectorant

PHENYLEPHRINE HCl - Nasal Decongestant

Relieves:
Headache, Fever, Sore throat, Minor aches
& pains, Cough, Chest congestion, Nasal/Sinus
congestion & Sinus pressure
Non-drowsy
Alcohol free
Antihistamine free

24 SOFTGELS

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

*This product is not
manufactured or distributed
by Procter & Gamble, owner
of the registered trademarks
Vicks® DayQuil® Severe Cold
& Flu.

* Please review the disclaimer below.