Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Aletris Combination 9203 (Aletris combination) NDC 63083-9203
Aletris farinosa root 4 [hp_X]/29.5mL + 11 more ingredients · Liquid · Oral · Professional Complementary Health Formulas
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 63083-9203-1 | 6308392030163083920301 | 29.5 mL in 1 BOTTLE, DROPPER (63083-9203-1)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)
- Aletris Combination 9203Suffix: 9203
- Generic name (nonproprietary)
- aletris combination
- Active ingredients
- Aletris farinosa root — 4 [hp_X]/29.5mLAnamirta cocculus fruit — 4 [hp_X]/29.5mLIron — 6 [hp_X]/29.5mLFerric cation — 6 [hp_X]/29.5mLFerrosoferric phosphate — 6 [hp_X]/29.5mLFerrous cation — 6 [hp_X]/29.5mLChamaelirium luteum root — 6 [hp_X]/29.5mLSodium chloride — 6 [hp_X]/29.5mLPicric acid — 6 [hp_X]/29.5mLSepia officinalis juice — 6 [hp_X]/29.5mLQuinine arsenite — 8 [hp_X]/29.5mLPotassium carbonate — 8 [hp_X]/29.5mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- Professional Complementary Health FormulasNDC labeler code 63083
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Other FDA classes
- Iron (Chemical structure)Phosphate Chelating Activity (Mechanism)
- Identifiers
- Product ID 63083-9203_eb4d236e-99a3-435e-b20b-b13d8b1f5086SPL ID eb4d236e-99a3-435e-b20b-b13d8b1f5086SPL set ID 87ae7310-927b-48fe-b659-6f93dad62363UNII O021JGR97X, 3E8XBL6YYK, E1UOL152H7, 91O4LML611, 91GQH8I5F7, GW89581OWR, DQV54Y5H3U, 451W47IQ8X, A49OS0F91S, QDL83WN8C2, 42QO5P0NLM, BQN1B9B9HA
- Pharmacologic class
- Antimalarial; Parenteral Iron Replacement; Phosphate Binder
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
N463083920301followed by a unit qualifier and the quantityPackage 63083-9203-01. 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 exhaustion, debility, weakness, or occasional headache.*
Excerpt only. Read the full label for complete information.
About NDC 63083-9203
- What is NDC 63083-9203?
- 63083-9203 is the product NDC for Aletris Combination 9203 (aletris combination), Aletris farinosa root 4 [hp_X]/29.5mL + 11 more ingredients liquid, listed with the FDA by Professional Complementary Health Formulas. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Aletris Combination 9203 (Aletris Combination).
- What is the active ingredient?
- Aletris farinosa root, Anamirta cocculus fruit, Iron, Ferric cation, Ferrosoferric phosphate, Ferrous cation, Chamaelirium luteum root, Sodium chloride, Picric acid, Sepia officinalis juice, Quinine arsenite, Potassium carbonate.
- Who is the labeler?
- Professional Complementary Health Formulas, NDC labeler code 63083. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Aletris Combination 9203?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.