FDA.reportPublic FDA data

HELIOX

Product NDC
10006-010
11-digit product format
100060010
Labeler code
10006
Product ID
10006-010_1366bd51-4f64-48d6-baa1-1fb402553331
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
HELIOX
Dosage form
GAS
Route
RESPIRATORY (INHALATION)
Labeler
Acetylene Oxygen Company
Marketing category
UNAPPROVED MEDICAL GAS
Marketing start
1936-01-01
Marketing end
0000-00-00
Substance
OXYGEN
Active strength
25 L/100L
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10006-010-012026-01-20C16284748780-1960f7f55-ca7c-8e05-e053-dbdaa90a074af0fd422f-ddbc-4259-90da-8822028210c7
10006-010-012019-10-29C16284748780-1960f7f55-ca7c-8e05-e053-dbdaa90a074af0fd422f-ddbc-4259-90da-8822028210c7

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
OXYGENACTIVE INGREDIENTS88TT14065HELIOX GAS [ACETYLENE OXYGEN COMPANY]1
OXYGENACTIVE MOIETYS88TT14065HELIOX GAS [ACETYLENE OXYGEN COMPANY]1
HELIUMINACTIVE INGREDIENT206GF3GB41HELIOX GAS [ACETYLENE OXYGEN COMPANY]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10006-010HELIOX GAS [ACETYLENE OXYGEN COMPANY]1Legacy NDC20110428_f0fd422f-ddbc-4259-90da-8822028210c7.zip