MedPath

Helium Oxygen

HELIUM OXYGEN 60 40

Approved
Approval ID

2c5a149b-1469-4b4e-b987-54986f028c2d

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Oct 12, 2010

Manufacturers
FDA

Airgas National Welders

DUNS: 003162310

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Helium Oxygen

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code11896-0019
Product Classification
G
Generic Name
Helium Oxygen
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateOctober 12, 2010
FDA Product Classification

INGREDIENTS (2)

HeliumActive
Quantity: 600 mL in 1 L
Code: 206GF3GB41
Classification: ACTIB
OxygenActive
Quantity: 400 mL in 1 L
Code: S88TT14065
Classification: ACTIB

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Helium Oxygen - FDA Drug Approval Details