MedPath

Oxygen

Oxygen Label

Approved
Approval ID

31bda224-d739-454c-9ab3-0aef40485b99

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Dec 4, 2009

Manufacturers
FDA

Home Care Medical, Inc

DUNS: 071147102

Products 1

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

Oxygen

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code58120-001
Product Classification
G
Generic Name
Oxygen
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateDecember 4, 2009
FDA Product Classification

INGREDIENTS (1)

OxygenActive
Quantity: 990 mL in 1 L
Code: S88TT14065
Classification: ACTIB

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