Uti Care Liquid
NDC Package 70163-0039-2

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

Package Information

Uti Care (barosma (betulina), dulcamara, equisetum hyemale, terebinthina, sarsaparilla (smilax regelii) triticum repens) liquids is adults and children 12 years and older: ■ take 15 drops under the tongue every hour for 4 hours or as needed. This formulation utilizes a liquid delivery system. Marketed by Naturalcare, this product is identified by NDC 70163-0039.

Identification & Billing

NDC Package Code
70163-0039-2
Package Description
1 BOTTLE, DROPPER in 1 CARTON / 30 mL in 1 BOTTLE, DROPPER (70163-0039-1)
Product Code
70163-0039
11-Digit Billing Format
70163003902

Clinical Specifications

Proprietary Name
Uti Care
Non-Proprietary Name
Barosma (betulina), Dulcamara, Equisetum Hyemale, Terebinthina, Sarsaparilla (smilax Regelii) Triticum Repens
Substance Name
Agathosma Betulina Leaf; Elymus Repens Root; Equisetum Hyemale Whole; Smilax Ornata Root; Solanum Dulcamara Top; Turpentine Oil
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)
Usage Information
Adults and children 12 years and older: ■ take 15 drops under the tongue every hour for 4 hours or as needed. Not recommended for children under 12 years of age.

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
03-20-2026
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 70163-0039-2 identifies a specific commercial package of 1 bottle, dropper in 1 carton / 30 ml in 1 bottle, dropper (70163-0039-1) of Uti Care, a human over the counter drug labeled by Naturalcare. This liquid is formulated for oral use and contains agathosma betulina leaf; elymus repens root; equisetum hyemale whole; smilax ornata root; solanum dulcamara top; turpentine oil 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 20, 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: 70163003902. 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)
70163-0039-2
11-Digit CMS (5-4-2)
70163-0039-02

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