Home NDC 59088-022 Boostervite
Product NDC 59088-022
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 Ingredient Strength FERROUS FUMARATE 18 mg/1 PANTOTHENIC ACID 50 mg/1 ORANGE JUICE 2.5 mg/1 BIOTIN 300 ug/1 RIBOFLAVIN 10 mg/1 NIACINAMIDE 10 mg/1 ASCORBIC ACID 100 mg/1 LEVOMEFOLATE CALCIUM 1000 ug/1 METHYLCOBALAMIN 100 ug/1 THIAMINE MONONITRATE 10 mg/1 PYRIDOXINE HYDROCHLORIDE 10 mg/1 CHOLECALCIFEROL 10 ug/1 BROCCOLI SPROUT 2.5 mg/1 PRUNUS CERASUS (BITTER CHERRY) FRUIT EXTRACT 2.5 mg/1 KALE 2.5 mg/1 WITHANIA SOMNIFERA ROOT 60 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 16 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 59088-022-54 59088002254 30 TABLET in 1 BOTTLE, PLASTIC (59088-022-54) 30 tablet 2026-06-19 No No Current