Nasalcrom Spray, Metered
NDC Package 52183-199-13

11-digit billing NDC: 52183019913

Package Information

Nasalcrom (cromolyn sodium) sprays is see package insert on how to use pumpparent or care provider must supervise the use of this product by young childrenadults and children 2 years and older:spray once into each nostril. 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

NDC Package Code
52183-199-13
Package Description
1 BOTTLE, PUMP in 1 CARTON / 200 SPRAY, METERED in 1 BOTTLE, PUMP
Product Code
11-Digit Billing Format
52183019913
RxNorm Crosswalk
  • 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

Proprietary Name
Nasalcrom
Non-Proprietary Name
Cromolyn Sodium
Substance Name
Cromolyn Sodium
Dosage Form
Spray, Metered - A non-pressurized dosage form consisting of valves which allow the dispensing of a specified quantity of spray upon each activation.
Administration Route
Nasal - Administration to the nose; administered by way of the nose.
Active Ingredient(s)
Usage Information
See package insert on how to use pumpparent or care provider must supervise the use of this product by young childrenadults and children 2 years and older:spray once into each nostril. Repeat 3-4 times a day (every 4-6 hours). If needed, may be used up to 6 times a day.use every day while in contact with the cause of your allergies (pollen, molds, pets, and dust)to prevent nasal allergy symptoms, use before contact with the cause of your allergies. For best results, start using up to one week before contact.if desired, you can use this product with other medicines, including other allergy medicines.children under 2 years: Do not use unless directed by a doctor.

Regulatory & Marketing

Labeler Name
Prestige Brands Holdings, Inc.
Product Type
Human Otc Drug
FDA Application #
ANDA075702
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
10-29-2009
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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.

1 BOTTLE, PUMP in 1 CARTON / 100 SPRAY, METERED in 1 BOTTLE, PUMP

* 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.

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:

10-Digit Format (5-3-2)
52183-199-13
11-Digit CMS (5-4-2)
52183-0199-13

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.