Allergy Relief Tablet
FDA Label NDC 72090-029

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Pioneer Life Sciences, Llc for the product Allergy Relief (NDC 72090-029). 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 ingredient (in each tablet), purpose, uses:, warnings:, keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Package Label

Pl0135-diphenhydramine-600ct-07.13.23-invahealth (Pl0135 Diphenhydramine 600ct 07.13.23 Invahealth)

Pl0135-diphenhydramine-600ct-07.13.23-invahealth (Pl0135 Diphenhydramine 600ct 07.13.23 Invahealth)

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