Helium

Helium

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

Company

Airgas Intermountain Inc

DUNS: 019714331

Effective Date

June 22, 2010

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Helium(992 mL in 1 L)

Manufacturing Establishments1

FDA-registered manufacturing facilities and establishments involved in the production, packaging, or distribution of this drug product.

Labeler

Airgas Intermountain Inc

DUNS Number

931891407

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

NDC Product Code

58420-004

Route of Administration

RESPIRATORY (INHALATION)

Effective Date

June 22, 2010

Ingredients

Code: 206GF3GB41Class: ACTIBQuantity: 992 mL in 1 L