Nasalcrom Spray, Metered
NDC Package 52183-199-13
Package Information
Nasalcrom (cromolyn sodium) sprays is a medication used to treat certain allergic eye conditions (vernal keratoconjunctivitis, vernal conjunctivitis, vernal keratitis). This formulation utilizes a spray, metered delivery system. Marketed by Prestige Brands Holdings, Inc., this product is identified by NDC 52183-199 and is authorized under FDA application ANDA075702.
Identification & Billing
- RxCUI: 1797851 - cromolyn sodium 5.2 MG/ACTUAT Metered Dose Nasal Spray
- RxCUI: 1797853 - Nasalcrom 5.2 MG/ACTUAT Metered Dose Nasal Spray
- RxCUI: 1797853 - cromolyn sodium 5.2 MG/ACTUAT Metered Dose Nasal Spray [Nasalcrom]
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 52183 - Prestige Brands Holdings, Inc.
- 52183-199 - Nasalcrom
- 52183-199-13 - 1 BOTTLE, PUMP in 1 CARTON / 200 SPRAY, METERED in 1 BOTTLE, PUMP
- 52183-199 - Nasalcrom
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (52183-199). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 52183-199-13 identifies a specific commercial package of 1 bottle, pump in 1 carton / 200 spray, metered in 1 bottle, pump of Nasalcrom, a human over the counter drug labeled by Prestige Brands Holdings, Inc.. This spray, metered is formulated for nasal use and contains cromolyn sodium as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Prestige Brands Holdings, Inc. on October 29, 2009. The current certification is valid through December 31, 2027.
What are the primary indications for this medication?
This medication is used to treat certain allergic eye conditions (vernal keratoconjunctivitis, vernal conjunctivitis, vernal keratitis). It prevents itching of the eyes that can occur with these conditions. Cromolyn is known as a mast cell stabilizer. It works by blocking certain natural substances (histamine, SRS-A) that cause allergic symptoms.
How is this Prestige Brands Holdings, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 52183019913. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.