What is NDC 59088-022?

59088-022 is the product NDC for Boostervite (multivitamin), Ferrous fumarate 18 mg/1 + 15 more ingredients tablet, listed with the FDA by PureTek Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.

What is the active ingredient?

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.

PureTek Corporation, NDC labeler code 59088. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Boostervite?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Boostervite NDC 59088-022 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59088-022Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59088-0022Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
59088-022-54	5908800225459088002254	30 TABLET in 1 BOTTLE, PLASTIC (59088-022-54)Marketed from Jun 19, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Boostervite
Generic name (nonproprietary): multivitamin
Active ingredients: Ferrous fumarate — 18 mg/1Pantothenic acid — 50 mg/1Orange juice — 2.5 mg/1Biotin — 300 ug/1Riboflavin — 10 mg/1Niacinamide — 10 mg/1Ascorbic acid — 100 mg/1Levomefolate calcium — 1000 ug/1Methylcobalamin — 100 ug/1Thiamine mononitrate — 10 mg/1Pyridoxine hydrochloride — 10 mg/1Cholecalciferol — 10 ug/1Broccoli sprout — 2.5 mg/1Prunus cerasus (Bitter cherry) fruit extract — 2.5 mg/1Kale — 2.5 mg/1Withania somnifera root — 60 mg/1
Dosage form: Tablet
Route: Oral
Labeler: PureTek CorporationNDC labeler code 59088
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Jun 19, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Analogs/Derivatives (Chemical/Ingredient)Ascorbic Acid (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Folic Acid (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)Vitamin B 6 (Chemical/Ingredient)Vitamin D (Chemical structure)
Identifiers: Product ID 59088-022_53efb4bb-24d4-8c55-e063-6394a90ab7b7SPL ID 53efb4bb-24d4-8c55-e063-6394a90ab7b7SPL set ID 53efbf65-8844-8486-e063-6394a90a51d3UNII R5L488RY0Q, 19F5HK2737, 5A9KE2L9L3, 6SO6U10H04, TLM2976OFR, 25X51I8RD4, PQ6CK8PD0R, A9R10K3F2F, BR1SN1JS2W, 8K0I04919X, 68Y4CF58BV, 1C6V77QF41, 128UH9LOAE, 1L29G6428X, 0Y3L4J38H1, V038D626IFUPC 0359088022542
Pharmacologic class: Folate Analog; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Vitamin B6 Analog; Vitamin C; Vitamin D

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N459088002254 followed by a unit qualifier and the quantity

Package 59088-0022-54. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jun 18, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE: Boostervite™ contains a combination of vitamins, minerals, and botanical extracts intended to supplement nutritional intake in patients with low energy associated with nutritional needs, under the supervision of a healthcare provider.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59088-022

What is NDC 59088-022?: 59088-022 is the product NDC for Boostervite (multivitamin), Ferrous fumarate 18 mg/1 + 15 more ingredients tablet, listed with the FDA by PureTek Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Boostervite (Multivitamin).
What is the active ingredient?: 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.
Who is the labeler?: PureTek Corporation, NDC labeler code 59088. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Boostervite?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Boostervite (Multivitamin) NDC 59088-022