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