NDC 17312-003

Ring Relief

Potassium Sulfate, Salicylic Acid, Silicon Dioxide, Calcium Sulfate Anhydrous, Quinine Sulfate, Allylthiourea

Ring Relief is a Oral Tablet, Multilayer in the Human Otc Drug category. It is labeled and distributed by Trp Company. The primary component is Potassium Sulfate; Salicylic Acid; Silicon Dioxide; Calcium Sulfate Anhydrous; Quinine Sulfate; Allylthiourea; Citrus Bioflavonoids; Ginkgo; Thiamine; Riboflavin; Niacinamide; Pantothenic Acid; Pyridoxine; Cyanocobalamin; Biotin; Folic Acid; Inositol; Zinc Picolinate; Ascorbic Acid.

• Product ID: 17312-003_747751c1-49c6-499c-9f28-93806138de11
• NDC: 17312-003
• Product Type: Human Otc Drug
• Proprietary Name: Ring Relief
• Generic Name: Potassium Sulfate, Salicylic Acid, Silicon Dioxide, Calcium Sulfate Anhydrous, Quinine Sulfate, Allylthiourea
• Dosage Form: Tablet, Multilayer
• Route of Administration: ORAL
• Marketing Start Date: 2006-06-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: TRP Company
• Substance Name: POTASSIUM SULFATE; SALICYLIC ACID; SILICON DIOXIDE; CALCIUM SULFATE ANHYDROUS; QUININE SULFATE; ALLYLTHIOUREA; CITRUS BIOFLAVONOIDS; GINKGO; THIAMINE; RIBOFLAVIN; NIACINAMIDE; PANTOTHENIC ACID; PYRIDOXINE; CYANOCOBALAMIN; BIOTIN; FOLIC ACID; INOSITOL; ZINC PICOLINATE; ASCORBIC ACID
• Active Ingredient Strength: 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; ug/1; ug/1; mg/1; mg/1; mg/1
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 17312-003-12

1 BOTTLE in 1 PACKAGE (17312-003-12) > 60 TABLET, MULTILAYER in 1 BOTTLE

• Marketing Start Date: 2006-06-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 17312-003-12 [17312000312]

Ring Relief TABLET, MULTILAYER

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2006-06-01
• Inactivation Date: 2019-11-13

Drug Details

Active Ingredients

Ingredient	Strength
POTASSIUM SULFATE	6 [hp_X]/1

OpenFDA Data

• SPL SET ID: 0a38f93c-cf61-48f0-be17-909c7a6485c6
• Manufacturer:
  • TRP Company
• UNII:
  • 25X51I8RD4
  • BD70459I50
  • 4L6452S749
  • 706IDJ14B7
  • ETJ7Z6XBU4
  • PQ6CK8PD0R
  • ALO92O31SE
  • KF7Z0E0Q2B
  • 19F5HK2737
  • O414PZ4LPZ
  • P6YC3EG204
  • TLM2976OFR
  • 1K573LC5TV
  • 935E97BOY8
  • X66NSO3N35
  • E934B3V59H
  • KV2JZ1BI6Z
  • 6SO6U10H04
  • 19FUJ2C58T
• PHarm Class EPC:
  • Vitamin B6 Analog [EPC]
• NUI Code:
  • N0000005657
  • N0000175452
  • N0000192800

NDC Crossover Matching brand name "Ring Relief" or generic name "Potassium Sulfate, Salicylic Acid, Silicon Dioxide, Calcium Sulfate Anhydrous, Quinine Sulfate, Allylthiourea"

NDC	Brand Name	Generic Name
17312-001	Ring Relief	Arnica Montana, Calcium Sulfide, Hypericum Perforatum, Lycopodium Clavatum Spore, Thiosinaminum, Mercurius Solubilis, Salicylic Acid, Silicon Dioxide, Allylthiourea
17312-003	Ring Relief	Potassium Sulfate, Salicylic Acid, Silicon Dioxide, Calcium Sulfate Anhydrous, Quinine Sulfate, Allylthiourea
17312-015	Ring Relief	ARNICA MONTANA - CALCIUM SULFIDE - HYPERICUM PERFORATUM - LYCOPODIUM CLAVATUM SPORE - MERCURIUS SOLUBILIS - SALICYLIC ACID - SILICON DIOXIDE - ALLYLTHIOUREA -
17312-023	Ring Relief	ARNICA MONTANA - CALCIUM SULFIDE - HYPERICUM PERFORATUM - LYCOPODIUM CLAVATUM SPORE - MERCURIUS SOLUBILIS - SALICYLIC ACID - SILICON DIOXIDE - ALLYLTHIOUREA -
17312-043	Ring Relief	ARNICA MONTANA - CALCIUM SULFIDE - HYPERICUM PERFORATUM - LYCOPODIUM CLAVATUM SPORE - MERCURIUS SOLUBILIS - SALICYLIC ACID - SILICON DIOXIDE - ALLYLTHIOUREA -