Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Nux Vomica Combination 9235 (nux vomica combination) NDC 63083-9235
Bryonia alba root 3 [hp_X]/29.5mL + 4 more ingredients · Liquid · Oral · Professional Complementary Health Formulas
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 63083-9235-1 | 63083923501 | 29.5 mL in 1 BOTTLE, DROPPER (63083-9235-1)Marketed from Aug 15, 1985 |
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)
- Nux Vomica Combination 9235Suffix: 9235
- Generic name (nonproprietary)
- nux vomica combination
- Active ingredients
- Bryonia alba root — 3 [hp_X]/29.5mLLycopodium clavatum spore — 3 [hp_X]/29.5mLStrychnos nux-vomica seed — 3 [hp_X]/29.5mLCitrullus colocynthis fruit pulp — 6 [hp_X]/29.5mLSulfur — 10 [hp_X]/29.5mL
- Dosage form
- Liquid
- Route
- Oral
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Other FDA classes
- Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
- Identifiers
- Product ID 63083-9235_c7cd08b0-dc77-44e8-a10f-79539d905a78SPL ID c7cd08b0-dc77-44e8-a10f-79539d905a78SPL set ID 28f6663d-0a00-4650-a84e-b625024687d3UNII T7J046YI2B, C88X29Y479, 269XH13919, 23H32AOH17, 70FD1KFU70
- 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
N463083923501followed by a unit qualifier and the quantityPackage 63083-9235-01. 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 the temporary relief of nausea, constipation, indigestion, heartburn, or irritability, especially after consumption of alcohol, caffeine, or nicotine.*
Excerpt only. Read the full label for complete information.