Carbon Dioxide
Air Source Industries Inc
Human Prescription Drug
NDC 10167-500Carbon Dioxide is a human prescription drug labeled by 'Air Source Industries Inc'. National Drug Code (NDC) number for Carbon Dioxide is 10167-500. This drug is available in dosage form of Gas. The names of the active, medicinal ingredients in Carbon Dioxide drug includes Carbon Dioxide - 99 L/100L . The currest status of Carbon Dioxide drug is Active.
Drug Information:
| Drug NDC: | 10167-500 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | Carbon Dioxide |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Product Type: | Human Prescription Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Carbon Dioxide |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Air Source Industries Inc |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Gas |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | CARBON DIOXIDE - 99 L/100L
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | RESPIRATORY (INHALATION)
|
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | NDA |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
| Marketing Start Date: | 01 Jan, 1992 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 22 Dec, 2025 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. |
| Application Number: | NDA205764 |
| This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null. |
| Listing Expiration Date: | 31 Dec, 2023 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | Air Source Industries Inc
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 309004
|
| The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| NUI: | N0000180185
N0000010258
|
| Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT). |
| UNII: | 142M471B3J
|
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
| Pharmacologic Class MOA: | X-Ray Contrast Activity [MoA]
|
| Mechanism of action of the drug—molecular, subcellular, or cellular functional activity—of the drug’s established pharmacologic class. Takes the form of the mechanism of action, followed by `[MoA]` (such as `Calcium Channel Antagonists [MoA]` or `Tumor Necrosis Factor Receptor Blocking Activity [MoA]`. |
| Pharmacologic Class EPC: | Radiographic Contrast Agent [EPC]
|
| Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`. |
| Pharmacologic Class: | Radiographic Contrast Agent [EPC]
X-Ray Contrast Activity [MoA]
|
| These are the reported pharmacological class categories corresponding to the SubstanceNames listed above. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 10167-500-01 | 940 L in 1 CYLINDER (10167-500-01) | 01 Jan, 1992 | N/A | No |
| 10167-500-02 | 1590 L in 1 CYLINDER (10167-500-02) | 01 Jan, 1992 | N/A | No |
| 10167-500-03 | 1232 L in 1 CYLINDER (10167-500-03) | 01 Jan, 1992 | N/A | No |
| 10167-500-04 | 4944 L in 1 CYLINDER (10167-500-04) | 01 Jan, 1992 | N/A | No |
| 10167-500-05 | 12300 L in 1 CYLINDER (10167-500-05) | 01 Jan, 1992 | N/A | No |
| 10167-500-06 | 147600 L in 1 DEWAR (10167-500-06) | 01 Jan, 1992 | N/A | No |
| 10167-500-07 | 94464 L in 1 DEWAR (10167-500-07) | 01 Jan, 1992 | N/A | No |
| 10167-500-08 | 13800 L in 1 CYLINDER (10167-500-08) | 01 Jan, 1992 | N/A | No |
| 10167-500-09 | 7570 L in 1 CYLINDER (10167-500-09) | 01 Jan, 1992 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Product Elements:
Carbon dioxide carbon dioxide carbon dioxide carbon dioxide
Package Label Principal Display Panel:
Carbon dioxide usp product label carbon dioxide usp un 1013 rx only e15 a air source industries, inc. 3976 cherry ave., long beach, ca 90807 in ca (800) 295-427 (562) 426-4017 non-flammablr gas 2 as-6 warning: administration of carcon dioxide may be hazardous or contraindicated. for use only by or under the supervision of a licensed practitioner who is experienced in the use and administration of carbon dioxide and is familiar with the indications, effects, dosages, methods, and frequency and duration of administration, and with the hazards, contraindications and side effects, and the precautions to be taken. warning: contains gas under pressure: may explode if heated. may displace oxygen and cause rapid suffocation. do not handle until all safety precautions have been read and understood. use and store only outdoors or in a well-ventilated place. use a back flow preventive device in the piping. use only with equipment rated for cylinder pressure. close valve after each use and when empty. protect from sunlight when ambient temperature exceeds 52°c (125°f). read and follow the safety data sheet (sds) before use. first aid: if inhaled: remove person to fresh air and keep comfortable for breathing. get medical advice/attention. cas 124-38-9 do not remove this product label airsource carbon dioxide sl
Carbon dioxide refrigerated liquid, usp product label carbon dioxide, refrigerated liquid, usp un 2187 rx only g08 as-31 a air source industries, inc. 3976 cherry ave., long beach, ca 90807 in ca (800) 295-427 (562) 426-4017 non-flammable 2 warning: always keep container in upright position. extremely cold liquid and gas pressure. can cause rapid suffocation and death without warning. can increase respiration and heart rate. may cause frostbite. avoid breathing gas. store and use with adequate ventilation. do not get liquid in eyes on skin, or clothing. for liquid withdraw, wear face shield and gloves. do not drop or handle container roughly. use suitable hand truck for container movement. container temperature should not exceed 125°f (52°c). close valve after each use and when empty. use in accordance with material safety data sheet. first aid: if inhaled, remove to fresh air. if not breathing, give artificial respiration. if breathing is difficult, give oxygen. call a physician. in case of frostbite, obtain medical treatment immediately. warning: administration of carbon dioxide may be hazardous or contraindicated. for use only by or under the supervision of a licensed practitioner who is experienced in the use and administration of carbon dioxide and is familiar with the indications, effects, dosages, methods, and frequency and duration of administration, and with the hazards, contraindications and side effects and the precautions to be taken. caution: federal law prohibits dispensing without prescription. caution: use no oil on valve or connections: transfiling of do not remove this product label airsource liq carbon dioxide