Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Dizziness HP NDC 44911-0187
Oyster shell calcium carbonate, Crude 30 [hp_X]/mL + 8 more ingredients · Liquid · Oral · Energique, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 44911-0187-1 | 44911018701 | 30 mL in 1 BOTTLE, DROPPER (44911-0187-1)Marketed from Jul 8, 2015 |
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)
- Dizziness HPSuffix: HP
- Generic name (nonproprietary)
- calcarea carbonica, chenopodium anthelminticum, cocculus indicus, conium maculatum, nux vomica, phosphorus, pulsatilla (pratensis), silicea, tabacum,
- Active ingredients
- Oyster shell calcium carbonate, Crude — 30 [hp_X]/mLDysphania ambrosioides — 30 [hp_X]/mLAnamirta cocculus seed — 30 [hp_X]/mLConium maculatum flowering top — 30 [hp_X]/mLStrychnos nux-vomica seed — 30 [hp_X]/mLPhosphorus — 30 [hp_X]/mLPulsatilla pratensis whole — 30 [hp_X]/mLSilicon dioxide — 30 [hp_X]/mLTobacco leaf — 30 [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
- Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
- Identifiers
- Product ID 44911-0187_f02fda13-544f-409a-bb7b-038d49cf4932SPL ID f02fda13-544f-409a-bb7b-038d49cf4932SPL set ID 0bf53ecc-c2ad-40b5-b921-7c10a1b00626UNII 2E32821G6I, 4H5RSU087I, 810258W28U, Q28R5GF371, 269XH13919, 27YLU75U4W, 8E272251DI, ETJ7Z6XBU4, 6YR2608RSU
- Pharmacologic class
- Non-Standardized Plant Allergenic Extract
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
N444911018701followed by a unit qualifier and the quantityPackage 44911-0187-01. 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: May temporarily relieve symptoms of dizziness and light-headedness.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Excerpt only. Read the full label for complete information.