Sinus Rx Liquid
NDC Package 69390-002-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Sinus Rx (calcarea carb, euphorbium, hydrastis, kali bic, kali iod, lycopodium, phosphorus, pulsatilla, thuja occ, sanguinaria) liquids is shake well and take 5 drops under tongue 3 times a day for 10 days. This formulation utilizes a liquid delivery system. Marketed by Miami Beach Pediatrics Pa, this product is identified by NDC 69390-002.

Identification & Billing

NDC Package Code
69390-002-01
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
69390-002
11-Digit Billing Format
69390000201

Clinical Specifications

Proprietary Name
Sinus Rx
Non-Proprietary Name
Calcarea Carb, Euphorbium, Hydrastis, Kali Bic, Kali Iod, Lycopodium, Phosphorus, Pulsatilla, Thuja Occ, Sanguinaria
Substance Name
Euphorbia Resinifera Resin; Goldenseal; Lycopodium Clavatum Spore; Oyster Shell Calcium Carbonate, Crude; Phosphorus; Potassium Dichromate; Potassium Iodide; Pulsatilla Vulgaris; Sanguinaria Canadensis Root; Thuja Occidentalis Leafy Twig
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Usage Information
Shake well and take 5 drops under tongue 3 times a day for 10 days. Take at least 15 minutes away from eating or drinking.

Regulatory & Marketing

Labeler Name
Miami Beach Pediatrics Pa
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
11-23-2015
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 69390-002-01 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Sinus Rx, a human over the counter drug labeled by Miami Beach Pediatrics Pa. This liquid is formulated for oral use and contains euphorbia resinifera resin; goldenseal; lycopodium clavatum spore; oyster shell calcium carbonate, crude; phosphorus; potassium dichromate; potassium iodide; pulsatilla vulgaris; sanguinaria canadensis root; thuja occidentalis leafy twig 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 Miami Beach Pediatrics Pa on November 23, 2015. The current certification is valid through December 31, 2026.

How is this Miami Beach Pediatrics Pa product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69390000201. 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)
69390-002-01
11-Digit CMS (5-4-2)
69390-0002-01

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