Citridrops Spray
NDC Package 83018-0003-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Citridrops (ascorbicum acidum, citrus limonun, pulsatilla, sinapis nigra, luffa operculata, berberis vulgaris, euphorbium officinarum, guaiacum, hepar sulphuris calcareum, mercurius sulphuratu ruber) sprays is for temporary relief of sinus congestion and inflammation caused by allergic reactions to common allergens and molds. This formulation utilizes a spray delivery system. Marketed by Micro Balance Health Products, this product is identified by NDC 83018-0003.

Identification & Billing

NDC Package Code
83018-0003-1
Package Description
29.5 mL in 1 BOTTLE, GLASS
Product Code
11-Digit Billing Format
83018000301

Clinical Specifications

Proprietary Name
Citridrops
Non-Proprietary Name
Ascorbicum Acidum, Citrus Limonun, Pulsatilla, Sinapis Nigra, Luffa Operculata, Berberis Vulgaris, Euphorbium Officinarum, Guaiacum, Hepar Sulphuris Calcareum, Mercurius Sulphuratu Ruber
Substance Name
Ascorbic Acid; Berberis Vulgaris Root Bark; Black Mustard Seed; Calcium Sulfide; Euphorbia Resinifera Resin; Guaiac; Lemon Juice; Luffa Operculata Whole; Mercuric Sulfide; Pulsatilla Pratensis
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route
Nasal - Administration to the nose; administered by way of the nose.
Usage Information
For temporary relief of sinus congestion and inflammation caused by allergic reactions to common allergens and molds

Regulatory & Marketing

Labeler Name
Micro Balance Health Products
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
02-21-2023
Listing Expiration
12-31-2026
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 83018-0003-1 identifies a specific commercial package of 29.5 ml in 1 bottle, glass of Citridrops, a human over the counter drug labeled by Micro Balance Health Products. This spray is formulated for nasal use and contains ascorbic acid; berberis vulgaris root bark; black mustard seed; calcium sulfide; euphorbia resinifera resin; guaiac; lemon juice; luffa operculata whole; mercuric sulfide; pulsatilla pratensis 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 Micro Balance Health Products on February 21, 2023. The current certification is valid through December 31, 2026.

How is this Micro Balance Health Products product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83018000301. 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 (5-4-1)
83018-0003-1
11-Digit CMS (5-4-2)
83018-0003-01

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