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
MOMORDICA CHARANTIA WHOLE68.7 mg/.6g
MORUS ALBA LEAF232.5 mg/.6g
PUERARIN84.6 mg/.6g
YEAST, UNSPECIFIED31.8 mg/.6g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii7BN8468162, 83M15WOS0F, M8YIA49Q2P, Z9W8997416, 3NY3SM6B8U

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

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