Weed Grass Antigens Liquid
NDC Package 44911-0553-1

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

Package Information

Weed Grass Antigens (allium cepa, arsenicum album, natrum muriaticum, nux vomica, pulsatilla (pratensis), abrotanum (artemisia abrotanum), absinthium, agrimonia eupatoria, flos, alfalfa, ambrosia artemisiaefolia, arundo mauritanica, bambusa arundinacea, cichorium intybus, flos, kentucky bluegrass, orchard grass, bermuda grass, johnson grass, rye grass, vernal grass, bahia grass, timothy grass, rumex crispus, sabadilla, sinapis arvensis, flos, solidago virgaurea, taraxacum officinale, trifolium pratense, trifolium repens,) liquids May temporarily relieve symptoms associated with weed and grass allergies, such as hay fever and runny nose and sneezing.****Claims based on traditional homeopathic practice, not accepted medical evidence. This formulation utilizes a liquid delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0553.

Identification & Billing

NDC Package Code
44911-0553-1
Package Description
60 mL in 1 BOTTLE, DROPPER
Product Code
44911-0553
11-Digit Billing Format
44911055301

Clinical Specifications

Proprietary Name
Weed Grass Antigens
Non-Proprietary Name
Allium Cepa, Arsenicum Album, Natrum Muriaticum, Nux Vomica, Pulsatilla (pratensis), Abrotanum (artemisia Abrotanum), Absinthium, Agrimonia Eupatoria, Flos, Alfalfa, Ambrosia Artemisiaefolia, Arundo Mauritanica, Bambusa Arundinacea, Cichorium Intybus, Flos, Kentucky Bluegrass, Orchard Grass, Bermuda Grass, Johnson Grass, Rye Grass, Vernal Grass, Bahia Grass, Timothy Grass, Rumex Crispus, Sabadilla, Sinapis Arvensis, Flos, Solidago Virgaurea, Taraxacum Officinale, Trifolium Pratense, Trifolium Repens,
Substance Name
Onion; Arsenic Trioxide; Sodium Chloride; Strychnos Nux-vomica Seed; Pulsatilla Pratensis Whole; Artemisia Abrotanum Flowering Top; Wormwood; Agrimonia Eupatoria Flower; Medicago Sativa Whole; Ambrosia Artemisiifolia Whole; Arundo Pliniana Root; Bambusa Bambos Leaf; Cichorium Intybus Flower; Poa Pratensis Pollen; Dactylis Glomerata Top; Cynodon Dactylon Pollen; Sorghum Halepense Pollen; Lolium Perenne Pollen; Anthoxanthum Odoratum Pollen; Paspalum Notatum Pollen; Phleum Pratense Top; Rumex Crispus Root; Schoenocaulon Officinale Seed; Sinapis Arvensis Flowering/fruiting Top; Solidago Virgaurea Flowering Top; Taraxacum Officinale; Trifolium Pratense Flower; Trifolium Repens Flower; Wyethia Helenioides Root
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)
Pharmacologic Class
Usage Information
May temporarily relieve symptoms associated with weed and grass allergies, such as hay fever and runny nose and sneezing.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. May temporarily relieve symptoms associated with weed and grass allergies, such as hay fever and runny nose and sneezing.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Regulatory & Marketing

Labeler Name
Energique, 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
07-31-2020
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 44911-0553-1 identifies a specific commercial package of 60 ml in 1 bottle, dropper of Weed Grass Antigens, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains onion; arsenic trioxide; sodium chloride; strychnos nux-vomica seed; pulsatilla pratensis whole; artemisia abrotanum flowering top; wormwood; agrimonia eupatoria flower; medicago sativa whole; ambrosia artemisiifolia whole; arundo pliniana root; bambusa bambos leaf; cichorium intybus flower; poa pratensis pollen; dactylis glomerata top; cynodon dactylon pollen; sorghum halepense pollen; lolium perenne pollen; anthoxanthum odoratum pollen; paspalum notatum pollen; phleum pratense top; rumex crispus root; schoenocaulon officinale seed; sinapis arvensis flowering/fruiting top; solidago virgaurea flowering top; taraxacum officinale; trifolium pratense flower; trifolium repens flower; wyethia helenioides root 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 Energique, Inc. on July 31, 2020. The current certification is valid through December 31, 2026.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 44911055301. 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)
44911-0553-1
11-Digit CMS (5-4-2)
44911-0553-01

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