Label: KALI SULPH- potassium sulfate tablet
- NDC Code(s): 54973-5230-1, 54973-5230-2
- Packager: Hyland's Inc.
- 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 December 19, 2022
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- DIRECTIONS
- INDICATIONS
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- PRINCIPAL DISPLAY PANEL - 500 Tablet Bottle Label
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INGREDIENTS AND APPEARANCE
KALI SULPH
potassium sulfate tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54973-5230 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM SULFATE (UNII: 1K573LC5TV) (SULFATE ION - UNII:7IS9N8KPMG) POTASSIUM SULFATE 6 [hp_X] Inactive Ingredients Ingredient Name Strength ACACIA (UNII: 5C5403N26O) LACTOSE (UNII: J2B2A4N98G) Product Characteristics Color white Score no score Shape ROUND Size 9mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54973-5230-1 500 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/01/1940 2 NDC:54973-5230-2 1000 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/01/1940 12/28/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/01/1940 Labeler - Hyland's Inc. (008316655) Establishment Name Address ID/FEI Business Operations Hyland's Inc. 008316655 manufacture(54973-5230) , pack(54973-5230) , label(54973-5230)