Daytime Cold, Nighttime Cold Kit
FDA Label NDC 41163-529

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by United Natural Foods, Inc. Dba Unfi for the product Daytime Cold, Nighttime Cold (NDC 41163-529). 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 caplet) (daytime cold multi-symptom), purpose, active ingredients(in each caplet) (nighttime cold multi-symptom), 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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