D-CAL SOYCAL- calcium carbonate, soy isoflavones and cholecalciferol tablet
A&Z Pharmaceutical, Inc.
Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Calcium 28.32 g
Soy Isoflavones 1.0 g
Vitamin D3 480
Increasing bone density, regulate blood fat.
Suitable for women with high blood lipid, middle, aged and elderly women
Unsuitable for children, pregnant women, lactating women
Storage and Shelf Life
24 months. Tightly closed and store in a dry place
1 caplet, one or two times daily
Pregnancy or Breast Feeding
Unsuitable for pregnant or lactating women
Keep Out of Reach of Children
Unsuitable for children
Calcium carbonate, soy isoflavones, vitamin D3, microcrystalline cellulose, croscarmellose sodium, magnesium stearate, silicon dioxide.
Call toll free in China: 800-810-9810
Country of Origin: USA
PRINCIPAL DISPLAY PANEL
| D-CAL SOYCAL |
calcium carbonate and soy isoflavones and vitamin d3 tablet
|Product Information |
|Product Type ||HUMAN OTC DRUG ||Item Code (Source) ||NDC:62211-127 |
|Route of Administration ||ORAL ||DEA Schedule || |
|Active Ingredient/Active Moiety |
|Ingredient Name ||Basis of Strength ||Strength |
|CALCIUM CARBONATE (CALCIUM CATION and CARBONATE ION ) ||CALCIUM CARBONATE ||28.32 g |
|SOY ISOFLAVONES (SOY ISOFLAVONES) ||SOY ISOFLAVONES ||1 g |
|CHOLECALCIFEROL (CHOLECALCIFEROL) ||CHOLECALCIFEROL ||480 ug |
|Inactive Ingredients |
|Ingredient Name ||Strength |
| CALCIUM CARBONATE || |
| SOY ISOFLAVONES || |
| CHOLECALCIFEROL || |
| CELLULOSE, MICROCRYSTALLINE || |
| CROSCARMELLOSE SODIUM || |
| MAGNESIUM STEARATE || |
| SILICON DIOXIDE || |
|Product Characteristics |
|Color ||orange ||Score ||no score |
|Shape ||OVAL ||Size ||18mm |
|Flavor || ||Imprint Code ||none |
|Contains || |
|# ||Item Code ||Package Description ||Multilevel Packaging |
| 1 ||NDC:62211-127-30 ||30 TABLET (TABLET) in 1 BOTTLE ||None |
| Marketing Information |
|Marketing Category ||Application Number or Monograph Citation ||Marketing Start Date ||Marketing End Date |
|OTC monograph final ||part331 ||01/22/2010 || |
|Labeler — A&Z Pharmaceutical, Inc.
|Registrant — A&Z Pharmaceutical, Inc. (926820705) |
| Establishment |
|Name ||Address ||ID/FEI ||Operations |
|A&Z Pharmaceutical, Inc. || ||926820705 ||manufacture (62211-127) |
Revised: 06/2012 A&Z Pharmaceutical, Inc.
Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.