Boostervite Tablet
NDC Package 59088-022-54
Package Information
Boostervite (multivitamin) tablets is a medication a multivitamin product used to treat or prevent vitamin deficiency due to poor diet, certain illnesses, or during pregnancy. This formulation utilizes a tablet delivery system. Marketed by Puretek Corporation, this product is identified by NDC 59088-022.
Identification & Billing
Clinical Specifications
- ASCORBIC ACID 100 mg/1
- BIOTIN 300 ug/1
- BROCCOLI SPROUT 2.5 mg/1
- CHOLECALCIFEROL 10 ug/1
- FERROUS FUMARATE 18 mg/1
- KALE 2.5 mg/1
- LEVOMEFOLATE CALCIUM 1000 ug/1
- METHYLCOBALAMIN 100 ug/1
- NIACINAMIDE 10 mg/1
- ORANGE JUICE 2.5 mg/1
- PANTOTHENIC ACID 50 mg/1
- PRUNUS CERASUS (BITTER CHERRY) FRUIT EXTRACT 2.5 mg/1
- PYRIDOXINE HYDROCHLORIDE 10 mg/1
- RIBOFLAVIN 10 mg/1
- THIAMINE MONONITRATE 10 mg/1
- WITHANIA SOMNIFERA ROOT 60 mg/1
- Allergens - [CS]
- Analogs/Derivatives - [Chemical/Ingredient]
- Ascorbic Acid - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Folate Analog - [EPC] (Established Pharmacologic Class)
- Folic Acid - [CS]
- Food Additives - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Vitamin B 6 - [Chemical/Ingredient]
- Vitamin B6 Analog - [EPC] (Established Pharmacologic Class)
- Vitamin C - [EPC] (Established Pharmacologic Class)
- Vitamin D - [CS]
- Vitamin D - [EPC] (Established Pharmacologic Class)
Regulatory & Marketing
Hierarchy Structure
- 59088 - Puretek Corporation
- 59088-022 - Boostervite
- 59088-022-54 - 30 TABLET in 1 BOTTLE, PLASTIC
- 59088-022 - Boostervite
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 59088-022-54 identifies a specific commercial package of 30 tablet in 1 bottle, plastic of Boostervite, a human prescription drug labeled by Puretek Corporation. This tablet is formulated for oral use and contains ascorbic acid; biotin; broccoli sprout; cholecalciferol; ferrous fumarate; kale; levomefolate calcium; methylcobalamin; niacinamide; orange juice; pantothenic acid; prunus cerasus (bitter cherry) fruit extract; pyridoxine hydrochloride; riboflavin; thiamine mononitrate; withania somnifera root as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Puretek Corporation on June 19, 2026. The current certification is valid through December 31, 2027.
What are the primary indications for this medication?
This medication is a multivitamin product used to treat or prevent vitamin deficiency due to poor diet, certain illnesses, or during pregnancy. Vitamins are important building blocks of the body and help keep you in good health.
How is this Puretek Corporation product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 59088002254. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.