Walgreens Day And Night Pack Kit
FDA Label NDC 0363-7570

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Walgreen Co for the product Walgreens Day And Night Pack (NDC 0363-7570). 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 day time (in each 20 ml), active ingredients for nighttime (in each 10 ml), purposes for daytime wal-tussin® dm, purpose for nighttime wal-tussin® dm, uses, do not us, 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.

If Pregnant Or Breast-Feeding,

DAYTIME

ask a health professional before use.

NIGHTTIME

ask a health professional before use

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