Sugar Control

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Sugar Control
Generic name
MORUS ALBA LEAF
Manufacturer
Bispit Canada Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
3df65e10-1eff-0fda-e063-6294a90af19e
SPL ID
3df65e10-1f00-0fda-e063-6294a90af19e
Version
1
Effective date
2025-09-04
Source export date
2026-10-27
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-27/d7629e6f844435cfe6cb0cf8c5341c46775ea16c5af42c77a22a2ffe820a2cd2/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 19:52:16
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

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.

Reported adverse events (FAERS/openFDA)#

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