High Potency Calcium

Manufacturer
Ulai Health LLC | Pharbest Pharmaceuticals, Inc.
Effective date
2019-07-23
Label type
DIETARY SUPPLEMENT
Version
1
Source
full-release
Hydrated at
2026-06-01 02:49:18

Label at a glance#

ProductHigh Potency Calcium
Active ingredientCHOLECALCIFEROL, CALCIUM CARBONATE
Label structure5 sections

Label contents#

Full prescribing information#

Supplement Facts

STATEMENT OF IDENTITY SECTION

Serving Size 1 Tablet

Servings Per Container 60

 Amount Per Serving    % Daily Value
 Vitamin D (as cholecalciferol)10 mcg (400 IU) 50%
 Calcium (as calcium carbonate) 600 mg 46%

Other ingredients: croscarmellose sodium, FD&C yellow #6, magnesium stearate, maltodextrin, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, talc, titanium dioxide

DOSAGE & ADMINISTRATION SECTION

Take one tablet up to three times daily with food or as directed by your doctor. Children under 4 years, ask a doctor.

Take with a full glass of water.

WARNINGS SECTION

If pregnant or breast-feeding, ask a health professional before use.

Package not child resistant.

Keep out of the reach of children.

SAFE HANDLING WARNING SECTION

Store at room temperature. Keep tightly closed in a cool dry place.

Questions or comments? (866) 562-2756 (Mon-Fri 8 AM to 4 PM EST)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PHARBEST

Manufactured in the USA

Compare to active ingredients of Caltrate® 600 + D3*

High Potency

Calcium

Calcium Supplement

600 mg + 10 mcg Vitamin D3

60 TABLETS

Ulai Calcium 600 mg + D 400 IU 60 ct labelUlai Calcium 600 mg + D 400 IU 60 ct label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
668292calcium carbonate 600 MG / vitamin D3 10 MCG (400 UNT) Oral TabletPSN1
668292calcium carbonate 600 MG / cholecalciferol 0.01 MG Oral TabletSCD1
668292calcium carbonate 600 MG / cholecalciferol 400 UNT Oral TabletSY1
668292calcium carbonate 600 MG / vitamin D3 10 MCG (400 UNT) Oral TabletSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CALCIUM CATION Pharmacologic Class Indexing3Indexing - Pharmacologic Class20230427
CHOLECALCIFEROL Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
594e2c86-3079-4e6e-96c9-48f7a8afc78dProduct name120230718
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
60c52429-fcef-eb54-2387-43bc9e4f296bProduct name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73057-402-07High Potency Calcium60 in 1 BOTTLE, PLASTICTABLET, FILM COATED601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73057-402HIGH POTENCY CALCIUM (CALCIUM 600MG AND 10 MCG VITAMIN D3) TABLET, FILM COATED [ULAI HEALTH LLC]11 package rows20190724_00d9e191-73d8-448f-974c-d1e73795cb72.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73057-40273057-402-07

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.