FDA.reportPublic FDA data

Sugar Control

Product NDC
85631-008
11-digit product format
856310008
Labeler code
85631
Product ID
85631-008_3df65e10-1f00-0fda-e063-6294a90af19e
Type
HUMAN OTC DRUG
Nonproprietary name
MORUS ALBA LEAF
Dosage form
TABLET
Route
ORAL
Labeler
Bispit Canada Ltd.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2025-09-04
Substance
ASTRAGALUS CRASSICARPUS WHOLE; MOMORDICA CHARANTIA WHOLE; MORUS ALBA LEAF; PUERARIN; YEAST, UNSPECIFIED
Active strength
132; 68.7; 232.5; 84.6; 31.8 mg/.6g; mg/.6g; mg/.6g; mg/.6g; mg/.6g
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Fungal Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Sugar Control
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ASTRAGALUS CRASSICARPUS WHOLE132 mg/.6g
PUERARIN68.7 mg/.6g
YEAST, UNSPECIFIED232.5 mg/.6g
MORUS ALBA LEAF84.6 mg/.6g
MOMORDICA CHARANTIA WHOLE31.8 mg/.6g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 5 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
7BN8468162Internal UNII lookup
Z9W8997416Internal UNII lookup
3NY3SM6B8UInternal UNII lookup
M8YIA49Q2PInternal UNII lookup
83M15WOS0FInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3df65e10-1eff-0fda-e063-6294a90af19eAvailable on FDA.report

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

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 (product): 85631-008

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85631-008-018563100080190 CAPSULE in 1 BOTTLE (85631-008-01) / .6 g in 1 CAPSULE90 capsule2025-09-04NoNoCurrent