What is NDC 44911-0109?

44911-0109 is the product NDC for Winter Blend, Echinacea angustifolia whole 1 [hp_X]/mL + 11 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

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).

What is the active ingredient?

Echinacea angustifolia whole, Arctostaphylos uva-ursi leaf, Baptisia tinctoria root, Convallaria majalis, Potassium chloride, Pinus sylvestris leafy twig, Thuja occidentalis leafy twig, Bryonia alba root, Crotalus horridus horridus venom, Lachesis muta venom, Selenium, Viscum album fruiting top.

Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Winter Blend?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Winter Blend NDC 44911-0109 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0109Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0109Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
44911-0109-1	4491101090144911010901	30 mL in 1 BOTTLE, DROPPER (44911-0109-1)Marketed from Oct 2, 2014

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Winter Blend
Generic name (nonproprietary): echinacea (angustifolia), uva-ursi, baptisia tinctoria, convallaria majalis, kali muriaticum, pinus sylvestris, thuja occidentalis, bryonia, crotalus horridus, lachesis mutus, selenium metallicum, viscum album
Active ingredients: Echinacea angustifolia whole — 1 [hp_X]/mLArctostaphylos uva-ursi leaf — 1 [hp_X]/mLBaptisia tinctoria root — 3 [hp_X]/mLConvallaria majalis — 6 [hp_X]/mLPotassium chloride — 6 [hp_X]/mLPinus sylvestris leafy twig — 6 [hp_X]/mLThuja occidentalis leafy twig — 6 [hp_X]/mLBryonia alba root — 12 [hp_X]/mLCrotalus horridus horridus venom — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLSelenium — 12 [hp_X]/mLViscum album fruiting top — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.NDC labeler code 44911
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 2, 2014
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers: Product ID 44911-0109_d4cc7185-15e0-4896-b776-24d0e3d194a9SPL ID d4cc7185-15e0-4896-b776-24d0e3d194a9SPL set ID ff696389-bad5-463a-be99-e92e86250e86UNII VB06AV5US8, 3M5V3D1X36, 5EF0HWI5WU, QHH4HVF5QE, 660YQ98I10, Q1RGP4UB73, 1NT28V9397, T7J046YI2B, YHA2XLJ956, VSW71SS07I, H6241UJ22B, BK9092J5MP
Pharmacologic class: Osmotic Laxative; Potassium Salt

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N444911010901 followed by a unit qualifier and the quantity

Package 44911-0109-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jul 12, 2024.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of various strains of influenza.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 44911-0109

What is NDC 44911-0109?: 44911-0109 is the product NDC for Winter Blend, Echinacea angustifolia whole 1 [hp_X]/mL + 11 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: 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).
What is the active ingredient?: Echinacea angustifolia whole, Arctostaphylos uva-ursi leaf, Baptisia tinctoria root, Convallaria majalis, Potassium chloride, Pinus sylvestris leafy twig, Thuja occidentalis leafy twig, Bryonia alba root, Crotalus horridus horridus venom, Lachesis muta venom, Selenium, Viscum album fruiting top.
Who is the labeler?: Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Winter Blend?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.