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  5. NDC Package Code: 75053-0009-1 Oxaltem

NDC Package 75053-0009-1 Oxaltem

Berberis Vulgaris,Oxalicum Acidum,Sanguinaria Canadensis,Chimaphila Umbellata,Calcarea - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
75053-0009-1
Package Description:
118 mL in 1 BOTTLE, DROPPER
Product Code:
75053-0009
Proprietary Name:
Oxaltem
Non-Proprietary Name:
Berberis Vulgaris, Oxalicum Acidum, Sanguinaria Canadensis, Chimaphila Umbellata, Calcarea Fluorica, Calcarea Silicata, Uricum Acidum, Calcarea Phosphorica, Parathormonum, Pyridoxinum Hydrochloricum
Substance Name:
Berberis Vulgaris Root Bark; Calcium Fluoride; Calcium Silicate; Chimaphila Umbellata Whole; Oxalic Acid; Parathyroid Hormone; Pyridoxine Hydrochloride; Sanguinaria Canadensis Whole; Tribasic Calcium Phosphate; Uric Acid
Usage Information:
Homeopathic medicine for the regulation of oxalate deposition and related dysfunctions of drainage.Claims based on homeopathic theory, not accepted medical evidence. Not FDA evaluated. Homeopathic medicine for the regulation of oxalate deposition and related dysfunctions of drainage.Claims based on homeopathic theory, not accepted medical evidence. Not FDA evaluated.
11-Digit NDC Billing Format:
75053000901
Product Type:
Human Otc Drug
Labeler Name:
Nucleic Products, Llc
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(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Pharmacologic Class(es):
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
01-31-2022
End Marketing Date:
07-26-2028
Exclude Flag:
N
Code Structure:

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 disclaimer below.

Frequently Asked Questions

What is NDC 75053-0009-1?

The NDC Packaged Code 75053-0009-1 is assigned to a package of 118 ml in 1 bottle, dropper of Oxaltem, a human over the counter drug labeled by Nucleic Products, Llc. The product's dosage form is liquid and is administered via oral form.

Is NDC 75053-0009 included in the NDC Directory?

Yes, Oxaltem with product code 75053-0009 is active and included in the NDC Directory. The product was first marketed by Nucleic Products, Llc on January 31, 2022.

What is the 11-digit format for NDC 75053-0009-1?

The 11-digit format is 75053000901. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-4-175053-0009-15-4-275053-0009-01