Helium
FDA Label NDC 58420-004

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Airgas Intermountain Inc for the product Helium (NDC 58420-004). 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 package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Package Label.Principal Display Panel


HELIUM, COMPRESSED USP
UN1046
NON-FLAMMABLE 2
30580 (05/02)

Rx only. CAUTION: Federal law prohibits dispensing without a prescription. WARNING: Administration of Helium may be hazardous or contraindicated. For use only by or under the supervision of a licensed practitioner who is experienced in the use and administration of Helium, and is familiar with the indications, effects, dosages, methods, and frequency and duration of administration, and with the hazards, contraindications and side effects, and the precautions to be taken.

CAUTION: HIGH PRESSURE GAS. CAN CAUSE RAPID SUFFOCATION. Store and use with adequate ventilation. Use equipment rated for cylinder pressure. Cylinder temperature should not exceed 52oC(125oF). Close valve after each use and when empty. Use in accordance with the Material Safety Data Sheet (MSDS). Inhaling Helium to alter the voice may prove fatal and should not be permitted. FIRST AID:   IF INHALED, remove to fresh air. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Call a physician.     C.A.S. : 7440-59-7        DO NOT REMOVE THIS PRODUCT LABEL.
AIRGAS PURITAN MEDICAL Distributed By: Airgas Intermountain, Inc. Denver, CO 80216 (303) 370-7800

Helium (Helium)

Helium (Helium)

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