Amalgam 6003 (amalgam) NDC 63083-6003

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-6003Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-6003Add 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
63083-6003-2	63083600302	59 mL in 1 BOTTLE, DROPPER (63083-6003-2)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): Amalgam 6003Suffix: 6003
Generic name (nonproprietary): amalgam
Active ingredients: Tilletia caries — 30 [hp_X]/59mLBos taurus gingiva — 30 [hp_X]/59mLBos taurus bone — 30 [hp_X]/59mLTreponema denticola — 30 [hp_X]/59mLIsatis tinctoria root — 30 [hp_X]/59mLSilver — 30 [hp_X]/59mLGold — 30 [hp_X]/59mLSilicon dioxide — 30 [hp_X]/59mLEpichlorohydrin — 30 [hp_X]/59mLFluorine — 30 [hp_X]/59mLMercurius solubilis — 30 [hp_X]/59mLXanthan gum — 30 [hp_X]/59mLNickel — 30 [hp_X]/59mLPalladium — 30 [hp_X]/59mLPlatinum — 30 [hp_X]/59mLZinc cation — 30 [hp_X]/59mLSodium fluoride — 30 [hp_X]/59mLTitanium — 30 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health Formulas
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 1984
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Decreased Copper Ion Absorption (Physiologic effect)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 63083-6003_2372e62a-e3fe-46a4-9acc-2c9df499085eSPL ID 2372e62a-e3fe-46a4-9acc-2c9df499085eSPL set ID 1af74f69-a23a-45a2-a20e-92bf8b0ccb22UNII C7000B9PQI, GJ2F3208WP, TRS31EO6ZN, 6TN2P16IOQ, 8S10GFI6DX, 3M4G523W1G, 79Y1949PYO, ETJ7Z6XBU4, 08OOR508C0, 284SYP0193, 324Y4038G2, TTV12P4NEE, 7OV03QG267, 5TWQ1V240M, 49DFR088MY, 13S1S8SF37, 8ZYQ1474W7, D1JT611TNE
Pharmacologic class: Copper Absorption Inhibitor; Non-Standardized Fungal 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

N463083600302 followed by a unit qualifier and the quantity

Package 63083-6003-02. 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 swollen, red, or tender gums, occasional bad breath, minor toothache, occasional headache, irritability, or fatigue due to sensitivity to or exposure to oral/dental materials.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)