Gingicaine Gel Variety Pak
FDA Label NDC 10129-070

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Gingi-pak A Division Of The Belport for the product Gingicaine Gel Variety Pak (NDC 10129-070). 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, inactive ingredients, warnings, precautions, consult a doctor promptly, allergy alert and contraindications, purpose, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.