NDC codes

FDA NDC Directory
Product NDC (as listed)55714-4814Labeler and product segments. Claims need a package NDC.
Product NDC at billing width55714-4814Add 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 NDC11-digit (billing)PackageCopy
55714-4814-1557144814015571448140130 mL in 1 BOTTLE, GLASS (55714-4814-1)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)
Exhaustion
Generic name (nonproprietary)
aconitum nap., adrenalinum, aralia quinquefolia, arnica, arsenicum alb., baptisia, bryonia, cantharis, chelidonium majus, cinchona, iodium, kali carb., kali iod., lachesis, lycopodium, lycopus virginicus, nat. mur., nux vom., phosphorus, pulsatilla, rhus toxicodendron, sabal, thyroidinum, echinacea, gingko, phytolacca.
Active ingredients
Aconitum napellus — 20 [hp_X]/mLEpinephrine — 20 [hp_X]/mLAmerican ginseng — 20 [hp_X]/mLArnica montana — 20 [hp_X]/mLArsenic trioxide — 20 [hp_X]/mLBaptisia tinctoria — 20 [hp_X]/mLBryonia alba root — 20 [hp_X]/mLLytta vesicatoria — 20 [hp_X]/mLChelidonium majus — 20 [hp_X]/mLCinchona officinalis bark — 20 [hp_X]/mLIodine — 20 [hp_X]/mLPotassium carbonate — 20 [hp_X]/mLPotassium iodide — 20 [hp_X]/mLLachesis muta venom — 20 [hp_X]/mLLycopodium clavatum spore — 20 [hp_X]/mLLycopus virginicus — 20 [hp_X]/mLSodium chloride — 20 [hp_X]/mLStrychnos nux-vomica seed — 20 [hp_X]/mLPhosphorus — 20 [hp_X]/mLAnemone pulsatilla — 20 [hp_X]/mLToxicodendron pubescens leaf — 20 [hp_X]/mLSaw palmetto — 20 [hp_X]/mLThyroid, Unspecified — 20 [hp_X]/mLEchinacea, Unspecified — 11 [hp_X]/mLGinkgo — 11 [hp_X]/mLPhytolacca americana root — 11 [hp_X]/mL
Dosage form
Liquid
Route
Oral
Labeler
Newton Laboratories, Inc.NDC labeler code 55714
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Agonists (Mechanism)Adrenergic beta-Agonists (Mechanism)Allergens (Chemical structure)Catecholamines (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers
Product ID 55714-4814_b592a02c-0487-f4ae-e053-2995a90a7f93SPL ID b592a02c-0487-f4ae-e053-2995a90a7f93SPL set ID 98fc56b6-afed-2cfd-e053-2995a90a59aeUNII U0NQ8555JD, YKH834O4BH, 8W75VCV53Q, O80TY208ZW, S7V92P67HO, 5K1UO2888Y, T7J046YI2B, 3Q034RO3BT, 7E889U5RNN, S003A158SB, 9679TC07X4, BQN1B9B9HA, 1C4QK22F9J, VSW71SS07I, C88X29Y479, TWH5125Q6F, 451W47IQ8X, 269XH13919, 27YLU75U4W, I76KB35JEV, 6IO182RP7A, J7WWH9M8QS, 0B4FDL9I6P, 4N9P6CC1DX, 19FUJ2C58T, 11E6VI8VEG
Pharmacologic class
Catecholamine; Non-Standardized Plant Allergenic Extract; alpha-Adrenergic Agonist; beta-Adrenergic Agonist

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

N455714481401 followed by a unit qualifier and the quantity

Package 55714-4814-01. 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 .

Indications (excerpt from the label)

INDICATIONS & USAGE SECTION Formulated for symptoms of mental and physical exhaustion, lack of concentration and apathy.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 55714-4814

What is NDC 55714-4814?
55714-4814 is the product NDC for Exhaustion, Aconitum napellus 20 [hp_X]/mL + 25 more ingredients liquid, listed with the FDA by Newton Laboratories, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Exhaustion (Aconitum nap., Adrenalinum, Aralia quinquefolia, Arnica, Arsenicum alb., Baptisia, Bryonia, Cantharis, Chelidonium majus, Cinchona, Iodium, Kali carb., Kali iod., Lachesis, Lycopodium, Lycopus virginicus, Nat. mur., Nux vom., Phosphorus, Pulsatilla, Rhus toxicodendron, Sabal, Thyroidinum, Echinacea, Gingko, Phytolacca.).
What is the active ingredient?
Aconitum napellus, Epinephrine, American ginseng, Arnica montana, Arsenic trioxide, Baptisia tinctoria, Bryonia alba root, Lytta vesicatoria, Chelidonium majus, Cinchona officinalis bark, Iodine, Potassium carbonate, Potassium iodide, Lachesis muta venom, Lycopodium clavatum spore, Lycopus virginicus, Sodium chloride, Strychnos nux-vomica seed, Phosphorus, Anemone pulsatilla, Toxicodendron pubescens leaf, Saw palmetto, Thyroid, Unspecified, Echinacea, Unspecified, Ginkgo, Phytolacca americana root.
Who is the labeler?
Newton Laboratories, Inc., NDC labeler code 55714. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Exhaustion?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

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