Label: TINNITUS RELIEF- cinchona officinalis bark,salicylic acid,quinine sulfate,ferrum phosphoricum,potassium chloride,calomel,allylthiourea,. pellet
- NDC Code(s): 61727-315-21
- Packager: Homeocare Laboratories
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated February 28, 2019
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- Active ingredients:
- Inactive ingredients:
- Purpose:
- Keep out of reach of children.
- Indications & Usage:
- Warnings:
- Dosage and Administration:
- Tinnitus Relief:
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INGREDIENTS AND APPEARANCE
TINNITUS RELIEF
cinchona officinalis bark,salicylic acid,quinine sulfate,ferrum phosphoricum,potassium chloride,calomel,allylthiourea,. pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61727-315 Route of Administration SUBLINGUAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (CINCHONA OFFICINALIS BARK - UNII:S003A158SB) CINCHONA OFFICINALIS BARK 9 [hp_C] in 4 g SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 15 [hp_C] in 4 g QUININE SULFATE (UNII: KF7Z0E0Q2B) (QUININE - UNII:A7V27PHC7A) QUININE SULFATE 9 [hp_C] in 4 g FERRUM PHOSPHORICUM (UNII: 91GQH8I5F7) (FERRUM PHOSPHORICUM - UNII:91GQH8I5F7) FERRUM PHOSPHORICUM 4 [hp_C] in 4 g POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CHLORIDE 4 [hp_C] in 4 g CALOMEL (UNII: J2D46N657D) (CALOMEL - UNII:J2D46N657D) CALOMEL 4 [hp_C] in 4 g ALLYLTHIOUREA (UNII: 706IDJ14B7) (ALLYLTHIOUREA - UNII:706IDJ14B7) ALLYLTHIOUREA 4 [hp_C] in 4 g Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) LACTOSE (UNII: J2B2A4N98G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61727-315-21 4 g in 1 TUBE; Type 0: Not a Combination Product 07/24/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/24/2012 Labeler - Homeocare Laboratories (088248828) Registrant - Homeocare Laboratories (088248828) Establishment Name Address ID/FEI Business Operations Homeocare Laboratories 088248828 manufacture(61727-315)