| Product NDC: | 10736-014 |
| Proprietary Name: | CARBON DIOXIDE |
| Non Proprietary Name: | CARBON DIOXIDE |
| Active Ingredient(s): | 995 mL/L & nbsp; CARBON DIOXIDE |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | GAS |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10736-014 |
| Labeler Name: | Medical-Technical Gases, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED MEDICAL GAS |
| Start Marketing Date: | 19630101 |
| Package NDC: | 10736-014-09 |
| Package Description: | 12376 L in 1 CYLINDER (10736-014-09) |
| NDC Code | 10736-014-09 |
| Proprietary Name | CARBON DIOXIDE |
| Package Description | 12376 L in 1 CYLINDER (10736-014-09) |
| Product NDC | 10736-014 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CARBON DIOXIDE |
| Dosage Form Name | GAS |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 19630101 |
| Marketing Category Name | UNAPPROVED MEDICAL GAS |
| Labeler Name | Medical-Technical Gases, Inc. |
| Substance Name | CARBON DIOXIDE |
| Strength Number | 995 |
| Strength Unit | mL/L |
| Pharmaceutical Classes | Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA] |