Label: 23% CALCIUM GLUCONATE liquid
- NDC Code(s): 50480-136-50
- Packager: Radix Laboratories, Inc.
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated November 13, 2014
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- • CONTENTS (grams/100ml):
- Inactives:
- Indications:
- Storage:
- Warnings:
- Dosage and administration:
- KEEP OUT OF REACH OF CHILDREN
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
23% CALCIUM GLUCONATE
23% calcium gluconate liquidProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:50480-136 Route of Administration ORAL 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 Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50480-136-50 12 in 1 CARTON 1 500 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/27/2013 Labeler - Radix Laboratories, Inc. (108500091)