Benadryl Allergy Ultratab Tablet, Film Coated
FDA Label NDC 73097-004

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Savings Distributors Llc for the product Benadryl Allergy Ultratab (NDC 73097-004). 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 drug facts, active ingredient (in each tablet), purpose, uses, 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.

Drug Facts

Purpose

Antihistamine

Package Label

Package Label (Benadrylallergy 25ct)

Package Label (Benadrylallergy 25ct)

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