Glucoseforce

Product NDC
43857-0648
11-digit product format
438570648
Labeler code
43857
Product ID
43857-0648_02c2483d-58b0-45a5-a221-5383dd06c10d
Type
HUMAN OTC DRUG
Nonproprietary name
Colchicum Autumnale, Lacticum Acidum, Lycopodium Clavatum, Phosphoricum Acidum, Phosphorus, Syzygium Jambolanum, Uranium Nitricum
Dosage form
LIQUID
Route
ORAL
Labeler
BioActive Nutritional, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2024-11-18
Substance
COLCHICUM AUTUMNALE BULB; LACTIC ACID, DL-; LYCOPODIUM CLAVATUM SPORE; PHOSPHORIC ACID; PHOSPHORUS; SYZYGIUM CUMINI SEED; URANYL NITRATE HEXAHYDRATE
Active strength
30; 30; 30; 30; 30; 30; 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

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

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Glucoseforce HPCOLCHICUM AUTUMNALE, LACTICUM ACIDUM, LYCOPODIUM CLAVATUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, SYZYGIUM JAMBOLANUM, URANIUM NITRICUMBioActive Nutritional, Inc.f1e89586-02ed-4b29-9902-12b17c01bee92026-03-09WarningsExact identifier
ndc (product): 43857-0648

Additional Listing Data#

Finished product
Yes
Brand name base
Glucoseforce
Brand name suffix
HP
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
COLCHICUM AUTUMNALE BULB30 [hp_X]/mL
LACTIC ACID, DL-30 [hp_X]/mL
LYCOPODIUM CLAVATUM SPORE30 [hp_X]/mL
PHOSPHORIC ACID30 [hp_X]/mL
PHOSPHORUS30 [hp_X]/mL
SYZYGIUM CUMINI SEED30 [hp_X]/mL
URANYL NITRATE HEXAHYDRATE30 [hp_C]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 7 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
993QHL78E6Internal UNII lookup
3B8D35Y7S4Internal UNII lookup
C88X29Y479Internal UNII lookup
E4GA8884NNInternal UNII lookup
27YLU75U4WInternal UNII lookup
820LSF646IInternal UNII lookup
3V057702FYInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
f1e89586-02ed-4b29-9902-12b17c01bee9Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43857-0648-1GlucoseforceHP30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43857-0648GLUCOSEFORCE HP (COLCHICUM AUTUMNALE, LACTICUM ACIDUM, LYCOPODIUM CLAVATUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, SYZYGIUM JAMBOLANUM, URANIUM NITRICUM) LIQUID [BIOACTIVE NUTRITIONAL, INC.]1Current NDC, 1 package rows20241120_f1e89586-02ed-4b29-9902-12b17c01bee9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
43857-0648-14385706480130 mL in 1 BOTTLE, DROPPER (43857-0648-1) 30 ml2024-11-18NoNoCurrent