Saline Nasal 1 Fl Oz
Sodium Chloride 2.65%
Alaina Healthcare Private Limited
Human Otc Drug
NDC 73492-701Saline Nasal 1 Fl Oz also known as Sodium Chloride 2.65% is a human otc drug labeled by 'Alaina Healthcare Private Limited'. National Drug Code (NDC) number for Saline Nasal 1 Fl Oz is 73492-701. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in Saline Nasal 1 Fl Oz drug includes Sodium Chloride - 2.65 mg/100mL . The currest status of Saline Nasal 1 Fl Oz drug is Active.
Drug Information:
| Drug NDC: | 73492-701 |
| 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: | Saline Nasal 1 Fl Oz |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Proprietary Name Base: | Saline Nasal |
| The base of the Brand/Proprietary name excluding its suffix. |
| Proprietary Name Suffix: | 1 fl oz |
| A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard. |
| Product Type: | Human Otc 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: | Sodium Chloride 2.65% |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Alaina Healthcare Private Limited |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Spray |
| 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: | SODIUM CHLORIDE - 2.65 mg/100mL
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | NASAL
|
| 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: | UNAPPROVED DRUG OTHER |
| 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: | 19 Nov, 2019 |
| 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. |
| 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: | ALAINA HEALTHCARE PRIVATE LIMITED
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 644148
|
| 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. |
| UPC: | 0050428618561
|
| UPC stands for Universal Product Code. |
| UNII: | 451W47IQ8X
|
| 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. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 73492-701-30 | 24 BOTTLE, SPRAY in 1 BOX (73492-701-30) / 30 mL in 1 BOTTLE, SPRAY | 19 Nov, 2019 | 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. |
Purpose:
Purpose nasal wash to flush allergens and dust from nasal passages
Product Elements:
Saline nasal 1 fl oz sodium chloride 2.65% benzalkonium chloride edetate disodium anhydrous water sodium chloride chloride ion
Indications and Usage:
Uses nasal congestion removes inhaled irritants (dust, dirt, pollen) moisturizes dry nasal passages
Warnings:
Warnings do not use if seal is broken or missing. warnings use of this product by more than one person may spread infection contents under pressure do not puncture or incinerate avoid spraying in eyes keep out of reach of children. the use of this dispenser by more than one person may spread infection.
Dosage and Administration:
Directions squeeze twice in each nostril as needed upright delivers a spray, horizontally a stream, upside down a drop take care not to aspirate nasal contents back into bottle if spray tip touches nose, rinse with hot water before replacing cap
Package Label Principal Display Panel:
Label untitled