OTC Medication Information: D-Cal SoyCal

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.

ACTIVE INGREDIENTS

Calcium 28.32 g

Soy Isoflavones 1.0 g

Vitamin D3 480

PURPOSES

Increasing bone density, regulate blood fat.

USES

Suitable for women with high blood lipid, middle, aged and elderly women

WARNINGS

Unsuitable for children, pregnant women, lactating women

Storage and Shelf Life

24 months. Tightly closed and store in a dry place

Directions

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

INACTIVE INGREDIENTS

Calcium carbonate, soy isoflavones, vitamin D3, microcrystalline cellulose, croscarmellose sodium, magnesium stearate, silicon dioxide.

QUESTIONS

Call toll free in China: 800-810-9810

Country of Origin: USA

PRINCIPAL DISPLAY PANEL

Dcal SoyCal
(click image for full-size original)

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
Packaging
# 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. (926820705)
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.

Medication Sections

Medication Information by RSS

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.

Terms of Use | Copyright © 2019. All Rights Reserved.