United States · FDA National Drug Code directory

Boostervite

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
59088-022_53efb4bb-24d4-8c55-e063-6394a90ab7b7
Product NDC
59088-022
Form
TABLET
Composition / generic term
Multivitamin
Labeler
PureTek Corporation
Marketing category
UNAPPROVED DRUG OTHER
Marketing start / end (source format)
20260619
Source listing expiry
20271231

Source-listed ingredients

  • 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

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE, PLASTIC (59088-022-54) · 59088-022-54

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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