Para-Si NDC 55714-4859

NDC codes

FDA NDC Directory

Product NDC (as listed)55714-4859Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55714-4859Add 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
55714-4859-1	55714485901	30 mL in 1 BOTTLE, GLASS (55714-4859-1)Marketed from Nov 26, 2024

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): Para-Si
Generic name (nonproprietary): juglans reg, abrotanum, aesculus hipp, allium sat, arsenicum alb, artemisia, baptisia, cina, cuprum met, filix mas, granatum, ipecac, lachesis, lycopodium, merc viv, naphthalinum, nat mur nux vom, pulsatilla, ratanhia, ruta, sabadilla, santoninum, silicea, spigelia anth, terebinthina, teucrium mar, thymolum, zingiber
Active ingredients: Artemisia abrotanum flowering top — 20 [hp_X]/mLHorse chestnut — 20 [hp_X]/mLGarlic — 20 [hp_X]/mLArsenic trioxide — 20 [hp_X]/mLArtemisia vulgaris root — 20 [hp_X]/mLBaptisia tinctoria root — 20 [hp_X]/mLArtemisia cina pre-flowering top — 20 [hp_X]/mLCopper — 20 [hp_X]/mLDryopteris filix-mas root — 20 [hp_X]/mLPunica granatum root bark — 20 [hp_X]/mLIpecac — 20 [hp_X]/mLLachesis muta venom — 20 [hp_X]/mLLycopodium clavatum spore — 20 [hp_X]/mLMercury — 20 [hp_X]/mLNaphthalene — 20 [hp_X]/mLSodium chloride — 20 [hp_X]/mLStrychnos nux-vomica seed — 20 [hp_X]/mLAnemone pulsatilla — 20 [hp_X]/mLKrameria lappacea root — 20 [hp_X]/mLRuta graveolens flowering top — 20 [hp_X]/mLSchoenocaulon officinale seed — 20 [hp_X]/mLSantonin — 20 [hp_X]/mLSilicon dioxide — 20 [hp_X]/mLSpigelia anthelmia — 20 [hp_X]/mLGinger — 20 [hp_X]/mLTurpentine oil — 20 [hp_X]/mLTeucrium marum — 20 [hp_X]/mLThymol — 20 [hp_X]/mLJuglans regia leaf — 11 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Newton Laboratories, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 26, 2024
Listing expires: Dec 31, 2026
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)Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Dietary Proteins (Chemical structure)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 55714-4859_27d587ec-b67e-ea05-e063-6394a90a9aacSPL ID 27d587ec-b67e-ea05-e063-6394a90a9aacSPL set ID 27d5997b-1cae-41c2-e063-6394a90ac74aUNII QG07G580U0, 3C18L6RJAZ, V1V998DC17, S7V92P67HO, 32MP823R8S, 5EF0HWI5WU, 28M1820ACT, 789U1901C5, C0ZK0RRF5X, CLV24I3T1D, 62I3C8233L, VSW71SS07I, C88X29Y479, FXS1BY2PGL, 2166IN72UN, 451W47IQ8X, 269XH13919, I76KB35JEV, P29ZH1A35Z, N94C2U587S, 6NAF1689IO, 1VL8J38ERO, ETJ7Z6XBU4, WYT05213GE, C5529G5JPQ, C5H0QJ6V7F, 10464S0TAA, 3J50XA376E, 85HKB87105
Pharmacologic class: Copper-containing Intrauterine Device; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

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

N455714485901 followed by a unit qualifier and the quantity

Package 55714-4859-01. 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 Nov 26, 2024.

Indications (excerpt from the label)

INDICATIONS & USAGE SECTION Formulated for symptoms such as bloating, fatigue, itching, nausea, teeth grinding, increased appetite, cramping and sluggish elimination.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)