Over-the-counter drug · UNAPPROVED HOMEOPATHIC
D03 Lvr-Drn NDC 63479-0403
Berberis vulgaris root bark 1 [hp_X]/mL + 14 more ingredients · Solution · Sublingual · Apex Energetics Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 63479-0403-1 | 63479040301 | 30 mL in 1 BOTTLE, GLASS (63479-0403-1)Marketed from Mar 15, 1993 |
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)
- D03 Lvr-DrnSuffix: LVR-DRN
- Generic name (nonproprietary)
- berberis vulgaris root bark, bryonia alba root, phenol, milk thistle, chelidonium majus, juniper berry, lycopodium clavatum spore, sodium phosphate, dibasic, heptahydrate, sodium sulfate, strychnos nux-vomica seed, phosphorus, lactic acid, l-, taraxacum officinale, viscum album fruiting top, and yucca filamentosa
- Active ingredients
- Berberis vulgaris root bark — 1 [hp_X]/mLBryonia alba root — 12 [hp_X]/mLPhenol — 12 [hp_X]/mLMilk thistle — 1 [hp_X]/mLChelidonium majus — 2 [hp_X]/mLJuniper berry — 1 [hp_X]/mLLycopodium clavatum spore — 30 [hp_X]/mLSodium phosphate, Dibasic, Heptahydrate — 15 [hp_X]/mLSodium sulfate — 10 [hp_X]/mLStrychnos nux-vomica seed — 30 [hp_X]/mLPhosphorus — 12 [hp_X]/mLLactic acid, L- — 12 [hp_X]/mLTaraxacum officinale — 12 [hp_X]/mLViscum album fruiting top — 2 [hp_X]/mLYucca filamentosa — 1 [hp_X]/mL
- Dosage form
- Solution
- Route
- Sublingual
- Labeler
- Apex Energetics 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)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
- Identifiers
- Product ID 63479-0403_0e76ea05-c3d0-8465-e063-6294a90a747fSPL ID 0e76ea05-c3d0-8465-e063-6294a90a747fSPL set ID f7eba30d-04f6-43b6-9020-052f1207e9f2UNII 1TH8Q20J0U, T7J046YI2B, 339NCG44TV, U946SH95EE, 7E889U5RNN, O84B5194RL, C88X29Y479, 70WT22SF4B, 0YPR65R21J, 269XH13919, 27YLU75U4W, F9S9FFU82N, 39981FM375, BK9092J5MP, T6VR38UJ9IUPC 0818960012564
- Pharmacologic class
- Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Osmotic Laxative
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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N463479040301followed by a unit qualifier and the quantityPackage 63479-0403-01. 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)
Uses: For temporary relief of minor: fatigue* headache* muscle ache* nervous irritability* restlessness* difficulty sleeping* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Excerpt only. Read the full label for complete information.