What is NDC 59088-003?

59088-003 is the product NDC for Bruselix Bruising, Arnica montana flower 50 mg/1 + 7 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?

Bruselix Bruising (Vitamin C, Zinc, Arnica Montana Extract, Bromelain, Diosmin, Rutin, Citrus Bioflavonoids, Hesperidin Methyl Chalcone).

What is the active ingredient?

Arnica montana flower, Stem bromelain, Sodium ascorbate, Hesperidin methylchalcone, Rutin, Diosmin, Hesperidin, Zinc picolinate.

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 Bruselix Bruising?

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.

Bruselix Bruising NDC 59088-003 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59088-003Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59088-0003Add 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
59088-003-81	59088000381	14 TABLET in 1 BOTTLE, PLASTIC (59088-003-81)Marketed from Oct 11, 2024

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): Bruselix Bruising
Generic name (nonproprietary): vitamin c, zinc, arnica montana extract, bromelain, diosmin, rutin, citrus bioflavonoids, hesperidin methyl chalcone
Active ingredients: Arnica montana flower — 50 mg/1Stem bromelain — 400 mg/1Sodium ascorbate — 120 mg/1Hesperidin methylchalcone — 25 mg/1Rutin — 50 mg/1Diosmin — 200 mg/1Hesperidin — 25 mg/1Zinc picolinate — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Puretek CorporationNDC labeler code 59088
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Oct 11, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Ascorbic Acid (Chemical structure)Decreased Copper Ion Absorption (Physiologic effect)
Identifiers: Product ID 59088-003_24245e80-529f-0542-e063-6394a90a1fb4SPL ID 24245e80-529f-0542-e063-6394a90a1fb4SPL set ID 24245e80-529f-0542-e063-6394a90a1fb4UNII OZ0E5Y15PZ, ZLM4P8929R, S033EH8359, 4T2GVA922X, 5G06TVY3R7, 7QM776WJ5N, E750O06Y6O, ALO92O31SE
Pharmacologic class: Copper Absorption Inhibitor; Vitamin C

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

N459088000381 followed by a unit qualifier and the quantity

Package 59088-0003-81. 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 Oct 11, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE: Bruselix™ Bruising Tablets are formulated to provide nutritional support during the body’s natural recovery process. They may be helpful for individuals experiencing bruising due to minor injuries, surgical procedures, or sensitive skin. The formula contains antioxidants, enzymes, and natural extracts that are traditionally used to support overall skin health and recovery.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59088-003

What is NDC 59088-003?: 59088-003 is the product NDC for Bruselix Bruising, Arnica montana flower 50 mg/1 + 7 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?: Bruselix Bruising (Vitamin C, Zinc, Arnica Montana Extract, Bromelain, Diosmin, Rutin, Citrus Bioflavonoids, Hesperidin Methyl Chalcone).
What is the active ingredient?: Arnica montana flower, Stem bromelain, Sodium ascorbate, Hesperidin methylchalcone, Rutin, Diosmin, Hesperidin, Zinc picolinate.
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 Bruselix Bruising?: 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.