Varico Liquid
NDC Package 44911-0667-1
Package Information
Varico (aesculus hippocastanum, calcarea fluorica, carbo vegetabilis, carduus marianus, hamamelis virginiana, lachesis mutus, lycopodium clavatum, paeonia officinalis, pulsatilla (pratensis), secale cornutum, sepia, staphysagria, zincum metallicum) 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 44911-0667.
Identification & Billing
Clinical Specifications
- ACTIVATED CHARCOAL 30 [hp_X]/mL
- CALCIUM FLUORIDE 30 [hp_X]/mL
- CLAVICEPS PURPUREA SCLEROTIUM 30 [hp_X]/mL
- DELPHINIUM STAPHISAGRIA SEED 30 [hp_X]/mL
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 30 [hp_X]/mL
- HORSE CHESTNUT 30 [hp_X]/mL
- LACHESIS MUTA VENOM 30 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 30 [hp_X]/mL
- MILK THISTLE 30 [hp_X]/mL
- PAEONIA OFFICINALIS ROOT 30 [hp_X]/mL
- PULSATILLA PRATENSIS WHOLE 30 [hp_X]/mL
- SEPIA OFFICINALIS JUICE 30 [hp_X]/mL
- ZINC 30 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0667 - Varico
- 44911-0667-1 - 30 mL in 1 BOTTLE, DROPPER
- 44911-0667 - Varico
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 44911-0667-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Varico HP, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains activated charcoal; calcium fluoride; claviceps purpurea sclerotium; delphinium staphisagria seed; hamamelis virginiana root bark/stem bark; horse chestnut; lachesis muta venom; lycopodium clavatum spore; milk thistle; paeonia officinalis root; pulsatilla pratensis whole; sepia officinalis juice; zinc 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 January 03, 2023. 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: 44911066701. 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.