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PRENATAL CHELATED MINERAL - 51861-102-88 - (CALCIUM CITRATE, CALCIUM CARBONATE, POTASSIUM IODIDE, MAGNESIUM CITRATE, ZINC CITRATE, COPPER GLUCONATE, and FERROUS FUMARATE)

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Drug Information of PRENATAL CHELATED MINERAL

Product NDC: 51861-102
Proprietary Name: PRENATAL CHELATED MINERAL
Non Proprietary Name: CALCIUM CITRATE, CALCIUM CARBONATE, POTASSIUM IODIDE, MAGNESIUM CITRATE, ZINC CITRATE, COPPER GLUCONATE, and FERROUS FUMARATE
Active Ingredient(s): 30; 32.5; .5; 7; 75; 75; 5    mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1 & nbsp;   CALCIUM CITRATE, CALCIUM CARBONATE, POTASSIUM IODIDE, MAGNESIUM CITRATE, ZINC CITRATE, COPPER GLUCONATE, and FERROUS FUMARATE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of PRENATAL CHELATED MINERAL

Product NDC: 51861-102
Labeler Name: USANA Health Sciences, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20120411

Package Information of PRENATAL CHELATED MINERAL

Package NDC: 51861-102-88
Package Description: 112 TABLET in 1 BOTTLE (51861-102-88)

NDC Information of PRENATAL CHELATED MINERAL

NDC Code 51861-102-88
Proprietary Name PRENATAL CHELATED MINERAL
Package Description 112 TABLET in 1 BOTTLE (51861-102-88)
Product NDC 51861-102
Product Type Name HUMAN OTC DRUG
Non Proprietary Name CALCIUM CITRATE, CALCIUM CARBONATE, POTASSIUM IODIDE, MAGNESIUM CITRATE, ZINC CITRATE, COPPER GLUCONATE, and FERROUS FUMARATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120411
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name USANA Health Sciences, Inc.
Substance Name CALCIUM CARBONATE; CALCIUM CITRATE; COPPER GLUCONATE; FERROUS FUMARATE; MAGNESIUM CITRATE; POTASSIUM IODIDE; ZINC CITRATE
Strength Number 30; 32.5; .5; 7; 75; 75; 5
Strength Unit mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1
Pharmaceutical Classes

Complete Information of PRENATAL CHELATED MINERAL


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