Urinary Hp Liquid
NDC Package 44911-0907-1
Package Information
Urinary Hp (berberis vulgaris, cantharis, causticum, clematis erecta, equisetum hyemale, lac caninum, lycopodium clavatum, mercurius vivus, pulsatilla (pratensis), sarsaparilla (smilax regelii), sepia, staphysagria) liquids is adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. This formulation utilizes a liquid delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0907.
Identification & Billing
Clinical Specifications
- BERBERIS VULGARIS ROOT BARK 30 [hp_X]/mL
- CANIS LUPUS FAMILIARIS MILK 30 [hp_X]/mL
- CAUSTICUM 30 [hp_X]/mL
- CLEMATIS RECTA FLOWERING TOP 30 [hp_X]/mL
- EQUISETUM HYEMALE WHOLE 30 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 30 [hp_X]/mL
- LYTTA VESICATORIA 30 [hp_X]/mL
- MERCURY 30 [hp_X]/mL
- PULSATILLA PRATENSIS WHOLE 30 [hp_X]/mL
- SEPIA OFFICINALIS JUICE 30 [hp_X]/mL
- SMILAX ORNATA WHOLE 30 [hp_X]/mL
- STAPHISAGRIA MACROSPERMA SEED 30 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0907 - Urinary Hp
- 44911-0907-1 - 30 mL in 1 BOTTLE, DROPPER
- 44911-0907 - Urinary Hp
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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 44911-0907-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Urinary Hp, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains berberis vulgaris root bark; canis lupus familiaris milk; causticum; clematis recta flowering top; equisetum hyemale whole; lycopodium clavatum spore; lytta vesicatoria; mercury; pulsatilla pratensis whole; sepia officinalis juice; smilax ornata whole; staphisagria macrosperma seed 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 April 02, 2026. The current certification is valid through December 31, 2027.
How is this Energique, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 44911090701. 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:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.