Immune Enhancement Liquescence 3029 NDC 63083-3029

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-3029Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-3029Add 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
63083-3029-4	63083302904	118 mL in 1 BOTTLE, DROPPER (63083-3029-4)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): Immune Enhancement Liquescence 3029Suffix: 3029
Generic name (nonproprietary): immune enhancement liquescence
Active ingredients: Echinacea angustifolia whole — 2 [hp_X]/118mLEchinacea purpurea whole — 2 [hp_X]/118mLPopulus balsamifera leaf bud — 2 [hp_X]/118mLGoldenseal — 5 [hp_X]/118mLCinchona officinalis bark — 6 [hp_X]/118mLCalcium sulfide — 6 [hp_X]/118mLIodine — 6 [hp_X]/118mLPotassium dichromate — 6 [hp_X]/118mLMercurius solubilis — 12 [hp_X]/118mL
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
Identifiers: Product ID 63083-3029_d28d6a9b-868a-4ebe-81e6-b4b8d8d71b3eSPL ID d28d6a9b-868a-4ebe-81e6-b4b8d8d71b3eSPL set ID 57cacb32-193b-4edf-a477-b6eb11a20283UNII VB06AV5US8, QI7G114Y98, 9CQ6C00G3C, ZW3Z11D0JV, S003A158SB, 1MBW07J51Q, 9679TC07X4, T4423S18FM, 324Y4038G2

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

N463083302904 followed by a unit qualifier and the quantity

Package 63083-3029-04. 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 minor aches, pains, or inflammation in the muscles or joints, sinus or nasal congestion, sore throat, hoarseness, chills, occasional headache, nausea, fatigue, or debility.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)