Multi-System NDC 55714-4813

NDC codes

FDA NDC Directory

Product NDC (as listed)55714-4813Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55714-4813Add 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
55714-4813-1	55714481301	30 mL in 1 BOTTLE, GLASS (55714-4813-1)Marketed from Sep 2, 2019

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): Multi-System
Generic name (nonproprietary): aconitum napellus, antimonium tartaricum, aralia quinquefolia, arnica montana, arsenicum album, baptisia tinctoria, bryonia, cantharis, chelidonium majus, cinchona officinalis, echinacea, iodium, kali carbonicum, kali iodatum, lachesis mutus, lycopodium clavatum, lycopus virginicus, natrum muriaticum, nux vomica, phosphorus, phytolacca decandra, pulsatilla, rhus toxicodendron, sabal serrulata, candida albicans, thyroidinum, ustilago maidis, aspergillus niger, cladosporium
Active ingredients: Aconitum napellus — 10 [hp_X]/mLPhosphorus — 10 [hp_X]/mLAmerican ginseng — 10 [hp_X]/mLArnica montana — 10 [hp_X]/mLArsenic trioxide — 10 [hp_X]/mLBaptisia tinctoria root — 10 [hp_X]/mLBryonia alba root — 10 [hp_X]/mLLytta vesicatoria — 10 [hp_X]/mLChelidonium majus — 10 [hp_X]/mLCinchona officinalis bark — 10 [hp_X]/mLEchinacea, Unspecified — 10 [hp_X]/mLIodine — 10 [hp_X]/mLPotassium carbonate — 10 [hp_X]/mLPotassium iodide — 10 [hp_X]/mLLachesis muta venom — 10 [hp_X]/mLLycopodium clavatum spore — 10 [hp_X]/mLLycopus virginicus — 10 [hp_X]/mLSodium chloride — 10 [hp_X]/mLStrychnos nux-vomica seed — 10 [hp_X]/mLSaw palmetto — 10 [hp_X]/mLAntimony potassium tartrate — 10 [hp_X]/mLUstilago maydis — 15 [hp_X]/mLCladosporium herbarum — 15 [hp_X]/mLAnemone pulsatilla — 10 [hp_X]/mLAspergillus niger var. Niger — 15 [hp_X]/mLCandida albicans — 15 [hp_X]/mLThyroid, Unspecified — 15 [hp_X]/mLPhytolacca americana root — 10 [hp_X]/mLToxicodendron pubescens leaf — 10 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Newton Laboratories, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 2, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Fungal Proteins (Chemical structure)Fungal Proteins (Chemical structure)Fungal Proteins (Chemical structure)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 55714-4813_b5ab37d8-22b7-62db-e053-2a95a90a3794SPL ID b5ab37d8-22b7-62db-e053-2a95a90a3794SPL set ID 9a65b40b-873b-346a-e053-2995a90aa968UNII U0NQ8555JD, 27YLU75U4W, 8W75VCV53Q, O80TY208ZW, S7V92P67HO, 5EF0HWI5WU, T7J046YI2B, 3Q034RO3BT, 7E889U5RNN, S003A158SB, 4N9P6CC1DX, 9679TC07X4, BQN1B9B9HA, 1C4QK22F9J, VSW71SS07I, C88X29Y479, TWH5125Q6F, 451W47IQ8X, 269XH13919, J7WWH9M8QS, DL6OZ476V3, 4K7Z7K7SWG, O64JF11198, I76KB35JEV, 9IOA40ANG6, 4D7G21HDBC, 0B4FDL9I6P, 11E6VI8VEG, 6IO182RP7A
Pharmacologic class: Non-Standardized Fungal 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

N455714481301 followed by a unit qualifier and the quantity

Package 55714-4813-01. 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 Dec 4, 2020.

Indications (excerpt from the label)

INDICATIONS & USAGE SECTION Formulated for symptoms such as muscle aches, cough, rash, headache, fever and chills.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)