FDA.reportPublic FDA data

Sugar Control

Manufacturer
Bispit Canada Ltd.
Effective date
2025-09-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:34:57

Label at a glance#

ProductSugar Control
Active ingredientASTRAGALUS CRASSICARPUS WHOLE, PUERARIN, YEAST, UNSPECIFIED, MORUS ALBA LEAF, MOMORDICA CHARANTIA WHOLE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Morus alba leaf、Momordica charantia whole.Puerarin、Astragalus crassicarpus whole、 Yeast.

INACTIVE INGREDIENT SECTION

Calcium carbonate.

OTC - PURPOSE SECTION

Assisting In Regulating Metabolic Functions

DOSAGE & ADMINISTRATION SECTION

Dosage: 2 tablets inthe morning and 2tablets in the evening

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep properly and out of reach of children.

WARNINGS SECTION

1. As a chronic metabolic issue, high bloodsugar requires long-term management inconjunction with diet control and a suitableexercise plan. A low-carbohydrate, low-sugardiet is recommended.2. This product is not a substitute formedication.Individuals on long-term medicationshould consult their physician beforediscontinuing any medication and shouldmonitor their daily blood sugar levels.3. This product is not recommended forindividuals with hypoglycemia.4. Keep properly and out of reach of children.

OTHER SAFETY INFORMATION

Storage:Store in a tightlysealed container in acool, dry place.

INDICATIONS & USAGE SECTION

Suitable for: People with diabetes.1. individuals who enjoy sweets, refinedcarbohydrates, and high-carb foods and wantto manage their daily sugar intake;2. Individuals with initially high blood glucoselevels as this product can help promote glucosemetabolism and balance blood sugar;3. Has an ameliorating effect for individualswith insulin resistance, hyperglycemia, anddiabetes.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85631-008-01Sugar Control0.6 g in 1 CAPSULETABLET0.61
85631-008-01Sugar Control90 in 1 BOTTLETABLET901

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85631-00885631-008-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ASTRAGALUS CRASSICARPUS WHOLE7BN8468162ACTIB
CALCIUM CARBONATEH0G9379FGKIACT
PUERARINZ9W8997416ACTIB
YEAST, UNSPECIFIED3NY3SM6B8UACTIB
MORUS ALBA LEAFM8YIA49Q2PACTIB
MOMORDICA CHARANTIA WHOLE83M15WOS0FACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sugar ControlMORUS ALBA LEAFBispit Canada Ltd.3df65e10-1eff-0fda-e063-6294a90af19e2025-09-04WarningsExact identifier
ndc (package): 85631-008-01
ndc (product): 85631-008
ndc11 (package): 85631000801
spl id: 3df65e10-1f00-0fda-e063-6294a90af19e
spl set id: 3df65e10-1eff-0fda-e063-6294a90af19e

Reported adverse events (FAERS/openFDA)#

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