NDC codes

FDA NDC Directory
Product NDC (as listed)55714-4857Labeler and product segments. Claims need a package NDC.
Product NDC at billing width55714-4857Add 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
55714-4857-1557144857015571448570130 mL in 1 BOTTLE, GLASS (55714-4857-1)Marketed from Jan 31, 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)
Tinnitus
Generic name (nonproprietary)
aconitum nap., baryta carb., baryta mur., capsicum, causticum, chenopodium anthelminticum, chininum sulphuricum, cinchona, glonoinum, graphites, hydrastis, kali bic., kali mur., lycopodium, phosphorus, pulsatilla, salicylicum ac., tabacum, thiosinaminum, viola odorata
Active ingredients
Aconitum napellus — 20 [hp_X]/mLBarium carbonate — 20 [hp_X]/mLBarium chloride dihydrate — 20 [hp_X]/mLCapsicum — 20 [hp_X]/mLCausticum — 20 [hp_X]/mLDysphania ambrosioides — 20 [hp_X]/mLQuinine sulfate — 20 [hp_X]/mLCinchona officinalis bark — 20 [hp_X]/mLNitroglycerin — 20 [hp_X]/mLGraphite — 20 [hp_X]/mLGoldenseal — 20 [hp_X]/mLPotassium dichromate — 20 [hp_X]/mLPotassium chloride — 20 [hp_X]/mLLycopodium clavatum spore — 20 [hp_X]/mLAnemone pulsatilla — 20 [hp_X]/mLSalicylic acid — 20 [hp_X]/mLTobacco leaf — 20 [hp_X]/mLAllylthiourea — 20 [hp_X]/mLViola odorata — 20 [hp_X]/mLPhosphorus — 20 [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
Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Nitrates (Chemical structure)Osmotic Activity (Mechanism)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Potassium Compounds (Chemical structure)Vasodilation (Physiologic effect)Vegetable Proteins (Chemical structure)
Identifiers
Product ID 55714-4857_10462abf-9261-c0fe-e063-6394a90a7a71SPL ID 10462abf-9261-c0fe-e063-6394a90a7a71SPL set ID 10462aaa-96d4-4ba3-e063-6294a90a7915UNII U0NQ8555JD, 6P669D8HQ8, EL5GJ3U77E, 00UK7646FG, DD5FO1WKFU, 4H5RSU087I, KF7Z0E0Q2B, S003A158SB, G59M7S0WS3, 4QQN74LH4O, ZW3Z11D0JV, T4423S18FM, 660YQ98I10, C88X29Y479, I76KB35JEV, O414PZ4LPZ, 6YR2608RSU, 706IDJ14B7, AET12U8B74, 27YLU75U4W
Pharmacologic class
Antimalarial; Nitrate Vasodilator; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Osmotic Laxative; Potassium Salt

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

N455714485701 followed by a unit qualifier and the quantity

Package 55714-4857-01. 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 associated symptoms such as ringing, buzzing, echoing, pressure, pain, throbbing and sensitivity to noise.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 55714-4857

What is NDC 55714-4857?
55714-4857 is the product NDC for Tinnitus, Aconitum napellus 20 [hp_X]/mL + 19 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?
Tinnitus (Aconitum nap., Baryta carb., Baryta mur., Capsicum, Causticum, Chenopodium anthelminticum, Chininum sulphuricum, Cinchona, Glonoinum, Graphites, Hydrastis, Kali bic., Kali mur., Lycopodium, Phosphorus, Pulsatilla, Salicylicum ac., Tabacum, Thiosinaminum, Viola odorata).
What is the active ingredient?
Aconitum napellus, Barium carbonate, Barium chloride dihydrate, Capsicum, Causticum, Dysphania ambrosioides, Quinine sulfate, Cinchona officinalis bark, Nitroglycerin, Graphite, Goldenseal, Potassium dichromate, Potassium chloride, Lycopodium clavatum spore, Anemone pulsatilla, Salicylic acid, Tobacco leaf, Allylthiourea, Viola odorata, Phosphorus.
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 Tinnitus?
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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