- DIRECTIONS
- PURPOSE
- ACTIVE INGREDIENT
-
Warnings
Do not use if imprinted cap band is broken or missing. If symptoms persist for more than seven days or worsen, contact a licensed health care provider.
Discontinue use if symptoms are accompanied by a high fever (over 101° F). Severe or persistent sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult physician promptly.
Do not use more than 2 days or administer to children under 3 years of age unless directed by physician.
- QUESTIONS?
- PRINCIPAL DISPLAY PANEL - 1000 Tablet Bottle Label
-
INGREDIENTS AND APPEARANCE
CALCIUM SULPHATE
calcium sulfate tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54973-3103 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM SULFATE (UNII: WAT0DDB505) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM SULFATE 30 [hp_X] Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) ACACIA (UNII: 5C5403N26O) Product Characteristics Color white Score no score Shape ROUND Size 5mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54973-3103-1 500 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/01/1940 2 NDC:54973-3103-2 1000 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/01/1940 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/01/1940 Labeler - Hyland's (028570695) Establishment Name Address ID/FEI Business Operations Standard Homeopathic Company 008316655 manufacture(54973-3103)