FDA.reportPublic FDA data

Boostervite

Product NDC
59088-022
Requested package NDC
59088-022-54
11-digit product format
590880022
Labeler code
59088
Product ID
59088-022_53efb4bb-24d4-8c55-e063-6394a90ab7b7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Multivitamin
Dosage form
TABLET
Route
ORAL
Labeler
PureTek Corporation
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2026-06-19
Substance
FERROUS FUMARATE; PANTOTHENIC ACID; ORANGE JUICE; BIOTIN; RIBOFLAVIN; NIACINAMIDE; ASCORBIC ACID; LEVOMEFOLATE CALCIUM; METHYLCOBALAMIN; THIAMINE MONONITRATE; PYRIDOXINE HYDROCHLORIDE; CHOLECALCIFEROL; BROCCOLI SPROUT; PRUNUS CERASUS (BITTER CHERRY) FRUIT EXTRACT; KALE; WITHANIA SOMNIFERA ROOT
Active strength
18; 50; 2.5; 300; 10; 10; 100; 1000; 100; 10; 10; 10; 2.5; 2.5; 2.5; 60 mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; ug/1; ug/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1
Pharmacologic classes
Allergens [CS], Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Folate Analog [EPC], Folic Acid [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vitamin B 6 [Chemical/Ingredient], Vitamin B6 Analog [EPC], Vitamin C [EPC], Vitamin D [CS], Vitamin D [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Boostervite
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
FERROUS FUMARATE18 mg/1
PANTOTHENIC ACID50 mg/1
ORANGE JUICE2.5 mg/1
BIOTIN300 ug/1
RIBOFLAVIN10 mg/1
NIACINAMIDE10 mg/1
ASCORBIC ACID100 mg/1
LEVOMEFOLATE CALCIUM1000 ug/1
METHYLCOBALAMIN100 ug/1
THIAMINE MONONITRATE10 mg/1
PYRIDOXINE HYDROCHLORIDE10 mg/1
CHOLECALCIFEROL10 ug/1
BROCCOLI SPROUT2.5 mg/1
PRUNUS CERASUS (BITTER CHERRY) FRUIT EXTRACT2.5 mg/1
KALE2.5 mg/1
WITHANIA SOMNIFERA ROOT60 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 16 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
R5L488RY0QInternal UNII lookup
19F5HK2737Internal UNII lookup
5A9KE2L9L3Internal UNII lookup
6SO6U10H04Internal UNII lookup
TLM2976OFRInternal UNII lookup
25X51I8RD4Internal UNII lookup
PQ6CK8PD0RInternal UNII lookup
A9R10K3F2FInternal UNII lookup
BR1SN1JS2WInternal UNII lookup
8K0I04919XInternal UNII lookup
68Y4CF58BVInternal UNII lookup
1C6V77QF41Internal UNII lookup
128UH9LOAEInternal UNII lookup
1L29G6428XInternal UNII lookup
0Y3L4J38H1Internal UNII lookup
V038D626IFInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
53efbf65-8844-8486-e063-6394a90a51d3Available on FDA.report

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
BoosterviteMULTIVITAMINPureTek Corporation53efbf65-8844-8486-e063-6394a90a51d32026-06-18Warnings, Adverse reactionsExact identifier
ndc (package): 59088-022-54
ndc (product): 59088-022
ndc11 (package): 59088002254

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
59088-022-545908800225430 TABLET in 1 BOTTLE, PLASTIC (59088-022-54) 30 tablet2026-06-19NoNoCurrent