Echinacea Combination 9222 (echinacea combination) NDC 63083-9222

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-9222Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-9222Add 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
63083-9222-1	63083922201	29.5 mL in 1 BOTTLE, DROPPER (63083-9222-1)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): Echinacea Combination 9222Suffix: 9222
Generic name (nonproprietary): echinacea combination
Active ingredients: Echinacea angustifolia whole — 2 [hp_X]/29.5mLAconitum napellus whole — 3 [hp_X]/29.5mLArnica montana whole — 4 [hp_X]/29.5mLBaptisia tinctoria whole — 4 [hp_X]/29.5mLSanguinaria canadensis root — 4 [hp_X]/29.5mLBryonia alba root — 6 [hp_X]/29.5mLEupatorium perfoliatum flowering top — 6 [hp_X]/29.5mLEuphorbia resinifera resin — 6 [hp_X]/29.5mLGelsemium sempervirens root — 6 [hp_X]/29.5mLPhytolacca americana root — 6 [hp_X]/29.5mLToxicodendron pubescens leaf — 6 [hp_X]/29.5mLSilver nitrate — 8 [hp_X]/29.5mLArsenic trioxide — 8 [hp_X]/29.5mLPhosphorus — 8 [hp_X]/29.5mLPulsatilla montana whole — 8 [hp_X]/29.5mLSulfur — 8 [hp_X]/29.5mLThuja occidentalis leaf — 8 [hp_X]/29.5mLCalcium sulfide — 10 [hp_X]/29.5mLLachesis muta venom — 10 [hp_X]/29.5mLZinc — 10 [hp_X]/29.5mLAristolochia clematitis root — 12 [hp_X]/29.5mLHaemophilus influenzae — 12 [hp_X]/29.5mLMercuric chloride — 12 [hp_X]/29.5mLCortisone acetate — 13 [hp_X]/29.5mLStaphylococcus aureus — 18 [hp_X]/29.5mLStreptococcus pyogenes — 18 [hp_X]/29.5mLRancid beef — 199 [hp_X]/29.5mL
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: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 63083-9222_ac519419-25d6-4e82-860c-7d1efaff70c1SPL ID ac519419-25d6-4e82-860c-7d1efaff70c1SPL set ID 430cc9f6-5565-4345-ac5f-d948fb3b14bdUNII VB06AV5US8, U0NQ8555JD, O80TY208ZW, 5K1UO2888Y, N9288CD508, T7J046YI2B, 1W0775VX6E, 1TI1O9028K, 639KR60Q1Q, 11E6VI8VEG, 6IO182RP7A, 95IT3W8JZE, S7V92P67HO, 27YLU75U4W, 24K790T39B, 70FD1KFU70, 0T0DQN8786, 1MBW07J51Q, VSW71SS07I, J41CSQ7QDS, ZY0NX0W00D, K738E2MB3I, 53GH7MZT1R, 883WKN7W8X, O478WX4004, LJ2LP0YL98, 29SUH5R3HU
Pharmacologic class: Corticosteroid

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

N463083922201 followed by a unit qualifier and the quantity

Package 63083-9222-01. 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 cold- and flu-like symptoms such as chills, muscle aches, cough, congestion, runny nose, occasional headache, or fatigue.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)