Saint Liquid
NDC Package 72784-101-01

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

Package Information

Saint (cough spray) liquids is see important warnings under "When using this product"adults & children 2 years & over:use 1 tablespoon of solution for each quart of water or 1½ teaspoonful of solution for each pint of wateradd solution directly to cold water only in a hot steam vaporizer (follow manufacturer's directions for using vaporizer)breathe in the medicated vaporsuse up to three times daily or as directed by a doctorchildren under 2 years: ask a doctor. This formulation utilizes a liquid delivery system. Marketed by Saint Medicine, Inc., this product is identified by NDC 72784-101 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
72784-101-01
Package Description
90 VIAL in 1 BOX / 5 mL in 1 VIAL
Product Code
72784-101
11-Digit Billing Format
72784010101

Clinical Specifications

Proprietary Name
Saint
Non-Proprietary Name
Cough Spray
Substance Name
Menthol
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
Respiratory (inhalation) - Administration within the respiratory tract by inhaling orally or nasally for local or systemic effect.
Active Ingredient(s)
MENTHOL 3.2 g/100mL
Usage Information
See important warnings under "When using this product"adults & children 2 years & over:use 1 tablespoon of solution for each quart of water or 1½ teaspoonful of solution for each pint of wateradd solution directly to cold water only in a hot steam vaporizer (follow manufacturer's directions for using vaporizer)breathe in the medicated vaporsuse up to three times daily or as directed by a doctorchildren under 2 years: ask a doctor

Regulatory & Marketing

Labeler Name
Saint Medicine, Inc.
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-20-2023
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 72784-101-01 identifies a specific commercial package of 90 vial in 1 box / 5 ml in 1 vial of Saint, a human over the counter drug labeled by Saint Medicine, Inc.. This liquid is formulated for respiratory (inhalation) use and contains menthol 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 Saint Medicine, Inc. on July 20, 2023. The current certification is valid through December 31, 2026.

How is this Saint Medicine, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72784010101. 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)
72784-101-01
11-Digit CMS (5-4-2)
72784-0101-01

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