NDC 10006-011

HELIOX

Heliox

HELIOX is a Respiratory (inhalation) Gas in the Human Prescription Drug category. It is labeled and distributed by Acetylene Oxygen Company. The primary component is Oxygen.

• Product ID: 10006-011_1366bd51-4f64-48d6-baa1-1fb402553331
• NDC: 10006-011
• Product Type: Human Prescription Drug
• Proprietary Name: HELIOX
• Generic Name: Heliox
• Dosage Form: Gas
• Route of Administration: RESPIRATORY (INHALATION)
• Marketing Start Date: 1936-01-01
• Marketing Category: UNAPPROVED MEDICAL GAS / UNAPPROVED MEDICAL GAS
• Labeler Name: Acetylene Oxygen Company
• Substance Name: OXYGEN
• Active Ingredient Strength: 30 L/100L
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 10006-011-01

6032 L in 1 CYLINDER (10006-011-01)

• Marketing Start Date: 1936-01-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10006-011-01 [10006001101]

HELIOX GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1936-01-01
• Inactivation Date: 2019-10-29

Drug Details

Active Ingredients

Ingredient	Strength
OXYGEN	30 L/100L

OpenFDA Data

• SPL SET ID: f0fd422f-ddbc-4259-90da-8822028210c7
• Manufacturer:
  • Acetylene Oxygen Company
• UNII:
  • S88TT14065
• RxNorm Concept Unique ID - RxCUI:
  • 413101

NDC Crossover Matching brand name "HELIOX" or generic name "Heliox"

NDC	Brand Name	Generic Name
10006-009	HELIOX	HELIOX
10006-010	HELIOX	HELIOX
10006-011	HELIOX	HELIOX
10297-007	Heliox	Heliox
10297-008	Heliox	Heliox
10297-070	Heliox	Heliox
10297-080	Heliox	Heliox
54776-001	Heliox	Heliox
54776-006	Heliox	Heliox
62273-007	Heliox	Heliox