Aum Alcohol Pad Swab
FDA Label NDC 73317-8801

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Slv Pharmaceuticals Llc Dba Aum Pharmaceuticals for the product Aum Alcohol Pad (NDC 73317-8801). 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, purpose, uses, warnings, do not use, stop use and ask a doctor if, discontinue use and consult a healthcare practitioner if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Package Label.Principal Display Panel

Label (Alco Pad Lbl)

Label (Alco Pad Lbl)

* Please review the disclaimer below.