Glycerin Suppository
FDA Label NDC 37808-398

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by H E B for the product Glycerin (NDC 37808-398). 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 suppository), purpose, uses, warnings, ask a doctor before using any laxative if you have, stop use and consult a doctor if you have, directions - single daily dose, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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