Throatspray
NDC Package 44911-0737-1
Package Information
Throatspray (echinacea (angustifolia), eugenia caryophyllata, glycerinum, myrrha, salvia officinalis, spilanthes oleracea, thymus serpyllum, baptisia tinctoria, phytolacca decandra, hydrastis canadensis, apis mellifica, belladonna, lachesis mutus, mercurius solubilis, hepar sulphuris calcareum) sprays is adults and children spray orally 4-6 times daily or as otherwise directed by a health care professional. This formulation utilizes a spray delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0737.
Identification & Billing
Clinical Specifications
- ACMELLA OLERACEA FLOWERING TOP 2 [hp_X]/mL
- APIS MELLIFERA 12 [hp_X]/mL
- ATROPA BELLADONNA 12 [hp_X]/mL
- BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL
- CALCIUM SULFIDE 15 [hp_X]/mL
- CLOVE 1 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA WHOLE 1 [hp_X]/mL
- GLYCERIN 1 [hp_X]/mL
- GOLDENSEAL 6 [hp_X]/mL
- LACHESIS MUTA VENOM 12 [hp_X]/mL
- MERCURIUS SOLUBILIS 12 [hp_X]/mL
- MYRRH 2 [hp_X]/mL
- PHYTOLACCA AMERICANA ROOT 4 [hp_X]/mL
- SAGE 2 [hp_X]/mL
- THYMUS SERPYLLUM WHOLE 6 [hp_X]/mL
- Allergens - [CS]
- Allergens - [CS]
- Bee Venoms - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Food Additives - [CS]
- Glycerol - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Standardized Insect Venom Allergenic Extract - [EPC] (Established Pharmacologic Class)
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0737 - Throatspray
- 44911-0737-1 - 60 mL in 1 BOTTLE, SPRAY
- 44911-0737 - Throatspray
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 44911-0737-1 identifies a specific commercial package of 60 ml in 1 bottle, spray of Throatspray, a human over the counter drug labeled by Energique, Inc.. This spray is formulated for oral use and contains acmella oleracea flowering top; apis mellifera; atropa belladonna; baptisia tinctoria root; calcium sulfide; clove; echinacea angustifolia whole; glycerin; goldenseal; lachesis muta venom; mercurius solubilis; myrrh; phytolacca americana root; sage; thymus serpyllum whole 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 29, 2025. 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: 44911073701. 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.