Ring Relief

Product NDC

17312-003

11-digit product format

173120003

Labeler code

17312

Product ID

17312-003_747751c1-49c6-499c-9f28-93806138de11

Type

HUMAN OTC DRUG

Nonproprietary name

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

Dosage form

TABLET, MULTILAYER

Route

ORAL

Labeler

TRP Company

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2006-06-01

Marketing end

0000-00-00

Substance

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 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

Current FDA listing

Historical FDA.report record