Grass Pollen Liquid
NDC Package 70163-0023-2

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

Package Information

Grass Pollen (adrenalinum, allium cepa, arsenicum iodatum, oats (avena sativa), brome grass (bromus inermis), bermuda grass (cynodon dactylon), orchard grass (dactylis glomerata), euphrasia officinalis, meadow grass (festuca elatior pratensis), histaminum hydrochloricum, perennial rye grass (lolium perenne), timothy grass (phleum pratense), sabadilla, sanguinaria canadensis, rye grass (secale cereale), johnson grass (sorghum halepense), wheat grass (triticum aestivum), corn (zea mays)) liquids is adults and children 12 years and over:■ take 15 drops under the tongue every 3-4 hours■ sensitive persons and asthma sufferers take 1-3 drops and wait 3 hours then continue with regular dosage provided■ if allergy or asthma symptoms develop, discontinue use. This formulation utilizes a liquid delivery system. Marketed by Naturalcare, this product is identified by NDC 70163-0023.

Identification & Billing

NDC Package Code
70163-0023-2
Package Description
1 BOTTLE, DROPPER in 1 CARTON / 30 mL in 1 BOTTLE, DROPPER (70163-0023-1)
Product Code
70163-0023
11-Digit Billing Format
70163002302

Clinical Specifications

Proprietary Name
Grass Pollen
Non-Proprietary Name
Adrenalinum, Allium Cepa, Arsenicum Iodatum, Oats (avena Sativa), Brome Grass (bromus Inermis), Bermuda Grass (cynodon Dactylon), Orchard Grass (dactylis Glomerata), Euphrasia Officinalis, Meadow Grass (festuca Elatior Pratensis), Histaminum Hydrochloricum, Perennial Rye Grass (lolium Perenne), Timothy Grass (phleum Pratense), Sabadilla, Sanguinaria Canadensis, Rye Grass (secale Cereale), Johnson Grass (sorghum Halepense), Wheat Grass (triticum Aestivum), Corn (zea Mays)
Substance Name
Arsenic Triiodide; Avena Sativa Pollen; Bromus Inermis Pollen; Cynodon Dactylon Pollen; Dactylis Glomerata Pollen; Epinephrine; Euphrasia Stricta; Histamine Dihydrochloride; Lolium Perenne Pollen; Lolium Pratense Pollen; Onion; Phleum Pratense Pollen; Sanguinaria Canadensis Root; Schoenocaulon Officinale Seed; Secale Cereale Pollen; Sorghum Halepense Pollen; Triticum Aestivum Pollen; Zea Mays Pollen
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
Adults and children 12 years and over:■ take 15 drops under the tongue every 3-4 hours■ sensitive persons and asthma sufferers take 1-3 drops and wait 3 hours then continue with regular dosage provided■ if allergy or asthma symptoms develop, discontinue use

Regulatory & Marketing

Labeler Name
Naturalcare
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
03-10-2026
Listing Expiration
12-31-2027
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 70163-0023-2 identifies a specific commercial package of 1 bottle, dropper in 1 carton / 30 ml in 1 bottle, dropper (70163-0023-1) of Grass Pollen, a human over the counter drug labeled by Naturalcare. This liquid is formulated for oral use and contains arsenic triiodide; avena sativa pollen; bromus inermis pollen; cynodon dactylon pollen; dactylis glomerata pollen; epinephrine; euphrasia stricta; histamine dihydrochloride; lolium perenne pollen; lolium pratense pollen; onion; phleum pratense pollen; sanguinaria canadensis root; schoenocaulon officinale seed; secale cereale pollen; sorghum halepense pollen; triticum aestivum pollen; zea mays pollen 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 Naturalcare on March 10, 2026. The current certification is valid through December 31, 2027.

How is this Naturalcare product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70163002302. 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)
70163-0023-2
11-Digit CMS (5-4-2)
70163-0023-02

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