Guna Allergy Solution/ Drops
FDA Label NDC 17089-461

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Guna Spa for the product Guna Allergy (NDC 17089-461). 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/purpose, warnings, directions, questions, indications & usage, inactive ingredient, purpose, otc - do not use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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