Body Balance Spray
NDC Package 44911-0635-1
Package Information
Body Balance (avena sativa, chlorophytum borivilianum, nuphar luteum, hypothalamus suis, orchitinum (suis), damiana, selenium metallicum, staphysagria, thuja occidentalis) sprays is temporarily relieves symptoms of low sexual energy and dysfunction which may be due to prostatitis, endometritis, endometriosis, low or poor sperm production, fatigue and decreased responsiveness.****Claims based on traditional homeopathic practice, not accepted medical evidence. This formulation utilizes a spray delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0635.
Identification & Billing
Clinical Specifications
- AVENA SATIVA FLOWERING TOP 3 [hp_X]/mL
- BOS TAURUS HYPOTHALAMUS 6 [hp_X]/mL
- CHLOROPHYTUM BORIVILIANUM WHOLE 3 [hp_X]/mL
- DELPHINIUM STAPHISAGRIA SEED 9 [hp_X]/mL
- NUPHAR LUTEA ROOT 6 [hp_X]/mL
- PUNICA GRANATUM ROOT BARK 6 [hp_X]/mL
- SELENIUM 9 [hp_X]/mL
- SUS SCROFA TESTICLE 6 [hp_X]/mL
- THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X]/mL
- TURNERA DIFFUSA LEAFY TWIG 9 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0635 - Body Balance
- 44911-0635-1 - 30 mL in 1 BOTTLE, SPRAY
- 44911-0635 - Body Balance
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 44911-0635-1 identifies a specific commercial package of 30 ml in 1 bottle, spray of Body Balance, a human over the counter drug labeled by Energique, Inc.. This spray is formulated for oral use and contains avena sativa flowering top; bos taurus hypothalamus; chlorophytum borivilianum whole; delphinium staphisagria seed; nuphar lutea root; punica granatum root bark; selenium; sus scrofa testicle; thuja occidentalis leafy twig; turnera diffusa leafy twig 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 March 16, 2021. 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: 44911063501. 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.