Winter Blend Liquid
NDC Package 44911-0109-1
Package Information
Winter Blend (echinacea (angustifolia), uva-ursi, baptisia tinctoria, convallaria majalis, kali muriaticum, pinus sylvestris, thuja occidentalis, bryonia, crotalus horridus, lachesis mutus, selenium metallicum, viscum album) liquids is for temporary relief of various strains of influenza.****Claims based on traditional homeopathic practice, not accepted medical evidence. This formulation utilizes a liquid delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0109.
Identification & Billing
Clinical Specifications
- ARCTOSTAPHYLOS UVA-URSI LEAF 1 [hp_X]/mL
- BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL
- BRYONIA ALBA ROOT 12 [hp_X]/mL
- CONVALLARIA MAJALIS 6 [hp_X]/mL
- CROTALUS HORRIDUS HORRIDUS VENOM 12 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA WHOLE 1 [hp_X]/mL
- LACHESIS MUTA VENOM 12 [hp_X]/mL
- PINUS SYLVESTRIS LEAFY TWIG 6 [hp_X]/mL
- POTASSIUM CHLORIDE 6 [hp_X]/mL
- SELENIUM 12 [hp_X]/mL
- THUJA OCCIDENTALIS LEAFY TWIG 6 [hp_X]/mL
- VISCUM ALBUM FRUITING TOP 12 [hp_X]/mL
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Potassium Compounds - [CS]
- Potassium Salt - [EPC] (Established Pharmacologic Class)
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0109 - Winter Blend
- 44911-0109-1 - 30 mL in 1 BOTTLE, DROPPER
- 44911-0109 - Winter Blend
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 44911-0109-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Winter Blend, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains arctostaphylos uva-ursi leaf; baptisia tinctoria root; bryonia alba root; convallaria majalis; crotalus horridus horridus venom; echinacea angustifolia whole; lachesis muta venom; pinus sylvestris leafy twig; potassium chloride; selenium; thuja occidentalis leafy twig; viscum album fruiting top 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 October 02, 2014. 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: 44911010901. 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.