Clearlife Extra Strength Tablet
NDC Package 62795-1050-2

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

Package Information

Clearlife Extra Strength (onion, ambrosia artemisiifolia whole, apis mellifera, arnica montana whole, euphrasia stricta, graphite, galphimia glauca flowering top, pulsatilla vulgaris whole, histamine dihydrochloride, pine tar, schoenocaulon officinale seed, sulfur, sulfuric acid, tellurium and thuja occidentalis leafy twig) tablets is for the temporary relief of minor allergy symptoms:Sinus Pressure, runny or itchy nose, Nasal congestion,Allergic Rhinitis, Sneezing, itchy or watery eyes, Allergy related headache, Itchy throat and skin. This formulation utilizes a tablet delivery system. Marketed by Medinatura Inc., this product is identified by NDC 62795-1050.

Identification & Billing

NDC Package Code
62795-1050-2
Package Description
1 BOTTLE in 1 CARTON / 60 TABLET in 1 BOTTLE
Product Code
11-Digit Billing Format
62795105002
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
1 EA

Clinical Specifications

Proprietary Name
Clearlife Extra Strength
Non-Proprietary Name
Onion, Ambrosia Artemisiifolia Whole, Apis Mellifera, Arnica Montana Whole, Euphrasia Stricta, Graphite, Galphimia Glauca Flowering Top, Pulsatilla Vulgaris Whole, Histamine Dihydrochloride, Pine Tar, Schoenocaulon Officinale Seed, Sulfur, Sulfuric Acid, Tellurium And Thuja Occidentalis Leafy Twig
Substance Name
Ambrosia Artemisiifolia Whole; Apis Mellifera; Arnica Montana; Euphrasia Stricta; Galphimia Glauca Flowering Top; Graphite; Histamine Dihydrochloride; Onion; Pine Tar; Pulsatilla Vulgaris Whole; Schoenocaulon Officinale Seed; Sulfur; Sulfuric Acid; Tellurium; Thuja Occidentalis Leafy Twig
Dosage Form
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route
Oral - Administration to or by way of the mouth.
Usage Information
For the temporary relief of minor allergy symptoms:Sinus Pressure, runny or itchy nose, Nasal congestion,Allergic Rhinitis, Sneezing, itchy or watery eyes, Allergy related headache, Itchy throat and skin.

Regulatory & Marketing

Labeler Name
Medinatura Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
01-06-2021
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 62795-1050-2 identifies a specific commercial package of 1 bottle in 1 carton / 60 tablet in 1 bottle of Clearlife Extra Strength, a human over the counter drug labeled by Medinatura Inc.. This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package. This tablet is formulated for oral use and contains ambrosia artemisiifolia whole; apis mellifera; arnica montana; euphrasia stricta; galphimia glauca flowering top; graphite; histamine dihydrochloride; onion; pine tar; pulsatilla vulgaris whole; schoenocaulon officinale seed; sulfur; sulfuric acid; tellurium; 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 Medinatura Inc. on January 06, 2021. The current certification is valid through December 31, 2026.

How is this Medinatura Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 62795105002. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 1 total billable units per package. 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)
62795-1050-2
11-Digit CMS (5-4-2)
62795-1050-02

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