Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Vitalizer NDC 43857-0629
Echinacea angustifolia whole 3 [hp_X]/mL + 13 more ingredients · Liquid · Oral · BioActive Nutritional, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 43857-0629-1 | 43857062901 | 30 mL in 1 BOTTLE, DROPPER (43857-0629-1)Marketed from Apr 6, 2023 |
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)
- Vitalizer
- Generic name (nonproprietary)
- echinacea (angustifolia), iodium, arsenicum album, aurum metallicum, calcarea fluorica, gallicum acidum, hekla lava, niccolum sulphuricum, phosphorus, sedum acre, sempervivum tectorum, senecio aureus, blatta americana, onosmodium virginianum
- Active ingredients
- Echinacea angustifolia whole — 3 [hp_X]/mLIodine — 6 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLGold — 12 [hp_X]/mLCalcium fluoride — 12 [hp_X]/mLGallic acid monohydrate — 12 [hp_X]/mLHekla lava — 12 [hp_X]/mLNickel sulfate hexahydrate — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLSedum acre whole — 12 [hp_X]/mLSempervivum tectorum leaf — 12 [hp_X]/mLPackera aurea whole — 12 [hp_X]/mLPeriplaneta americana — 16 [hp_X]/mLOnosmodium virginianum — 30 [hp_C]/mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- BioActive Nutritional, 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)Insect Proteins (Chemical structure)
- Identifiers
- Product ID 43857-0629_ec54a5b1-a400-4022-8452-cbb85f0396c3SPL ID ec54a5b1-a400-4022-8452-cbb85f0396c3SPL set ID a643abc6-5367-4b34-848a-83bdb6ddd87dUNII VB06AV5US8, 9679TC07X4, S7V92P67HO, 79Y1949PYO, O3B55K4YKI, 48339473OT, C21158IIRK, JC9WZ4FK68, 27YLU75U4W, 2496VW6S9J, 3DGJ7BUA01, 5WS1632J8W, 2RQ1L9N089, 604NK4250S
- Pharmacologic class
- Non-Standardized Insect Allergenic Extract; Standardized Chemical Allergen
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
N443857062901followed by a unit qualifier and the quantityPackage 43857-0629-01. 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 fatigue, weakness after exhausting diseases, headaches and sensitivity to light and noise.
Excerpt only. Read the full label for complete information.