Label: CALCIUM GLUCONATE injection, solution
- NDC Code(s): 50989-882-16
- Packager: Vedco
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated August 22, 2019
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- ACTIVE INGREDIENTS:
- INACTIVE INGREDIENTS
- INDICATIONS
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DOSAGE AND ADMINISTRATION:
Cattle: 200 to 500 mL.
Administer intravnously or intraperitoneally.
Solution should be warmed to body temperature and administered slowly. This product is sterile in unopened container. It contains no preservative. Use entire content when first opened. It should be handled under aseptic conditions. If there is no apparent improvement in animal's conditionwithin 24 hours, consult a veterinarian.
- STORAGE
- WARNINGS
- VETERINARY INDICATIONS
- SAFE HANDLING WARNING
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CALCIUM GLUCONATE
calcium gluconate injection, solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:50989-882 Route of Administration INTRAVENOUS, INTRAPERITONEAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM GLUCONATE (UNII: SQE6VB453K) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM GLUCONATE 23 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BORIC ACID (UNII: R57ZHV85D4) 3.5 g in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50989-882-16 500 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/22/2019 Labeler - Vedco (021634266) Registrant - Vedco (021634266)