Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Tinnitus NDC 55714-4857
Aconitum napellus 20 [hp_X]/mL + 19 more ingredients · Liquid · Oral · Newton Laboratories, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 55714-4857-1 | 5571448570155714485701 | 30 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
N455714485701followed by a unit qualifier and the quantityPackage 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.
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.