NDC 10006-008

HELIUM

Helium

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

• Product ID: 10006-008_73d34d59-69b0-4bc0-b31d-617aa0d5b3fc
• NDC: 10006-008
• Product Type: Human Prescription Drug
• Proprietary Name: HELIUM
• Generic Name: Helium
• 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: HELIUM
• Active Ingredient Strength: 99 L/100L
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 10006-008-02

425 L in 1 CYLINDER (10006-008-02)

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

NDC SPL Data Element Entries

NDC 10006-008-01 [10006000801]

HELIUM GAS

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

NDC 10006-008-05 [10006000805]

HELIUM GAS

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

NDC 10006-008-02 [10006000802]

HELIUM GAS

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

NDC 10006-008-06 [10006000806]

HELIUM GAS

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

NDC 10006-008-03 [10006000803]

HELIUM GAS

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

NDC 10006-008-04 [10006000804]

HELIUM 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
HELIUM	99 L/100L

OpenFDA Data

• SPL SET ID: 8c473d18-b656-4e00-8fbc-6e1128d41254
• Manufacturer:
  • Acetylene Oxygen Company
• UNII:
  • 206GF3GB41
• RxNorm Concept Unique ID - RxCUI:
  • 310693

NDC Crossover Matching brand name "HELIUM" or generic name "Helium"

NDC	Brand Name	Generic Name
10006-008	HELIUM	HELIUM
10014-004	Helium	Helium
10018-9505	Helium	Helium
10167-300	HELIUM	HELIUM
10297-006	Helium	Helium
10678-004	Helium	Helium
10736-020	Helium	Helium
11054-004	HELIUM	HELIUM
11324-005	Helium	Helium
12213-710	Helium	Helium
14961-005	Helium	Helium
17575-005	Helium	Helium
21220-121	Helium	Helium
25543-011	Helium	Helium
25373-010	Helium	Helium
42602-002	HELIUM	HELIUM
46123-008	Helium	Helium
48883-006	Helium	Helium
54416-005	Helium	Helium
55037-501	Helium	Helium
57472-007	Helium	Helium
58420-004	Helium	Helium
58789-005	Helium	Helium
59579-005	Helium	Helium
61095-300	Helium	Helium
48273-011	Helium	Helium
73468-002	Helium	Helium
51486-020	Helium	Helium