NDC 37205-223 Cromolyn Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 37205 - Cardinal Health
- 37205-223 - Cromolyn Sodium
Product Packages
NDC Code 37205-223-61
Package Description: 1 BOTTLE in 1 CARTON / 26 mL in 1 BOTTLE
Price per Unit: $0.26292 per ML
Product Details
What is NDC 37205-223?
What are the uses for Cromolyn Sodium?
Which are Cromolyn Sodium UNII Codes?
The UNII codes for the active ingredients in this product are:
- CROMOLYN SODIUM (UNII: Q2WXR1I0PK)
- CROMOLYN (UNII: Y0TK0FS77W) (Active Moiety)
Which are Cromolyn Sodium Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Cromolyn Sodium?
- RxCUI: 1797851 - cromolyn sodium 5.2 MG/ACTUAT Metered Dose Nasal Spray
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Patient Education
Cromolyn Sodium Nasal Solution
Cromolyn is used to prevent and treat stuffy nose, sneezing, runny nose, and other symptoms caused by allergies. It works by preventing the release of substances that cause inflammation (swelling) in the air passages of the nose. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".