Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Winter Blend NDC 44911-0109
Echinacea angustifolia whole 1 [hp_X]/mL + 11 more ingredients · Liquid · Oral · Energique, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 44911-0109-1 | 44911010901 | 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.
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- 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
N444911010901followed by a unit qualifier and the quantityPackage 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 .
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.