What is NDC 63083-9232?

63083-9232 is the product NDC for Magnesium Combination 9232 (magnesium combination), Artemisia annua flowering top 3 [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?

Magnesium Combination 9232 (Magnesium Combination).

What is the active ingredient?

Artemisia annua flowering top, Passiflora incarnata flowering top, Amanita muscaria fruiting body, Ammonium bromide, Aconitum napellus whole, Atropine sulfate, Citrullus colocynthis fruit pulp, Cupric cation, Gelsemium sempervirens root, Hyoscyamus niger, Magnesium phosphate, Dibasic trihydrate, Veratrum album root.

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 Magnesium Combination 9232?

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.

Magnesium Combination 9232 NDC 63083-9232

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-9232Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-9232Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
63083-9232-1	6308392320163083923201	29.5 mL in 1 BOTTLE, DROPPER (63083-9232-1)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): Magnesium Combination 9232Suffix: 9232
Generic name (nonproprietary): magnesium combination
Active ingredients: Artemisia annua flowering top — 3 [hp_X]/29.5mLPassiflora incarnata flowering top — 3 [hp_X]/29.5mLAmanita muscaria fruiting body — 4 [hp_X]/29.5mLAmmonium bromide — 4 [hp_X]/29.5mLAconitum napellus whole — 6 [hp_X]/29.5mLAtropine sulfate — 6 [hp_X]/29.5mLCitrullus colocynthis fruit pulp — 6 [hp_X]/29.5mLCupric cation — 6 [hp_X]/29.5mLGelsemium sempervirens root — 6 [hp_X]/29.5mLHyoscyamus niger — 6 [hp_X]/29.5mLMagnesium phosphate, Dibasic trihydrate — 6 [hp_X]/29.5mLVeratrum album root — 6 [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: Aug 15, 1984
Listing expires: Dec 31, 2027
Other FDA classes: Cholinergic Antagonists (Mechanism)Cholinergic Muscarinic Antagonists (Mechanism)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 63083-9232_b72006c9-04da-4aea-aba9-949d15be3b67SPL ID b72006c9-04da-4aea-aba9-949d15be3b67SPL set ID 4d99b3ec-724f-4385-ae5e-83389bb0c8feUNII 0UQK6O82OW, CLF5YFS11O, DIF093I037, R0JB3224WS, U0NQ8555JD, 03J5ZE7KA5, 23H32AOH17, 8CBV67279L, 639KR60Q1Q, 4WRK2153H3, HF539G9L3Q, QNS6W5US1Z
Pharmacologic class: Anticholinergic; Calculi Dissolution Agent; Cholinergic Muscarinic Antagonist; 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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N463083923201 followed by a unit qualifier and the quantity

Package 63083-9232-01. 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 Jan 8, 2026.

Indications (excerpt from the label)

INDICATIONS For the temporary relief of muscular spasms, aches, or pain.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-9232

What is NDC 63083-9232?: 63083-9232 is the product NDC for Magnesium Combination 9232 (magnesium combination), Artemisia annua flowering top 3 [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?: Magnesium Combination 9232 (Magnesium Combination).
What is the active ingredient?: Artemisia annua flowering top, Passiflora incarnata flowering top, Amanita muscaria fruiting body, Ammonium bromide, Aconitum napellus whole, Atropine sulfate, Citrullus colocynthis fruit pulp, Cupric cation, Gelsemium sempervirens root, Hyoscyamus niger, Magnesium phosphate, Dibasic trihydrate, Veratrum album root.
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 Magnesium Combination 9232?: 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.

Magnesium Combination 9232 (Magnesium combination) NDC 63083-9232