61727-315 : Tinnitus Relief Sublingual Pellet


NDC: 61727-315
Labeler: Homeocare Laboratories
Product Type: Human OTC Drug
Drug Name: Tinnitus Relief
Dosage Form: Sublingual Pellet
Rev. Date: 


NDC Package Codes:

  • 61727-315-21: 4 G IN 1 TUBE (61727‑315‑21)

Active Ingredients:

  • Cinchona Officinalis Bark
  • Salicylic Acid
  • Quinine Sulfate
  • Ferrum Phosphoricum
  • Potassium Chloride
  • Calomel
  • Allylthiourea

Dosage Strength:

  • 9 [hp_C]/4g
  • 15 [hp_C]/4g
  • 9 [hp_C]/4g
  • 4 [hp_C]/4g
  • 4 [hp_C]/4g
  • 4 [hp_C]/4g
  • 4 [hp_C]/4g

Pharmaceutical Classes:

  • Antimalarial [EPC]
  • Increased Large Intestinal Motility [PE]
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
  • Osmotic Activity [MoA]
  • Osmotic Laxative [EPC]
  • Potassium Compounds [CS]
  • Potassium Salt [EPC]

Related Products:

Based on records with the same trade name.
  • 43689-0009 Tinnitus Relief (Oyster Shell Calcium Carbonate, Crude 6 [hp_x] / Quinine Sulfate 6 [hp_x] / Potassium Carbonate 6 [hp_x] / Lycopodium Clavatum Spore 6 [hp_x] / Salicylic Acid 6 [hp_x]) by The Magni Company
  • 57955-0275 Tinnitus Relief Oral Liquid by King Bio Inc.
  • 60512-9054 Tinnitus Relief Oral Pellet by Homeolab USA Inc.

NDC QR Code

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NDC 61727-315 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.