What is NDC 59469-301?

59469-301 is the product NDC for Akutur, Benzoic acid 4 [hp_X]/50mL + 7 more ingredients solution/ drops, listed with the FDA by PEKANA Nautrheilmittel GmbH. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Akutur (BENZOIC ACID, NITRIC ACID, Apis mellifera, Lytta vesicatoria, Populus tremuloides Bark, ANEMONE PRATENSIS Flowering TOP, GINGER, and Solidago virgaurea Flowering Top).

What is the active ingredient?

Benzoic acid, Nitric acid, Apis mellifera, Lytta vesicatoria, Populus tremuloides bark, Pulsatilla pratensis flowering top, Ginger, Solidago virgaurea flowering top.

PEKANA Nautrheilmittel GmbH, NDC labeler code 59469. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Akutur?

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.

Akutur NDC 59469-301 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-301Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0301Add 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
59469-301-10	5946903011059469030110	1 BOTTLE, GLASS in 1 BOX (59469-301-10) / 50 mL in 1 BOTTLE, GLASSMarketed from Jun 24, 2019

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): Akutur
Generic name (nonproprietary): benzoic acid, nitric acid, apis mellifera, lytta vesicatoria, populus tremuloides bark, anemone pratensis flowering top, ginger, and solidago virgaurea flowering top
Active ingredients: Benzoic acid — 4 [hp_X]/50mLNitric acid — 6 [hp_X]/50mLApis mellifera — 3 [hp_X]/50mLLytta vesicatoria — 4 [hp_X]/50mLPopulus tremuloides bark — 2 [hp_X]/50mLPulsatilla pratensis flowering top — 4 [hp_X]/50mLGinger — 3 [hp_X]/50mLSolidago virgaurea flowering top — 2208 mg/50mL
Dosage form: Solution/ drops
Route: Oral
Labeler: PEKANA Nautrheilmittel GmbHNDC labeler code 59469
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 24, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Ammonium Ion Binding Activity (Mechanism)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 59469-301_4d19cb5d-3526-4bd8-af97-8ace1615350bSPL ID 4d19cb5d-3526-4bd8-af97-8ace1615350bSPL set ID 7facf36e-c26e-4bc3-a4c1-74e9409f2535UNII 8SKN0B0MIM, 411VRN1TV4, 7S82P3R43Z, 3Q034RO3BT, 5543O0CEID, 29NVY5MR1A, C5529G5JPQ, 5405K23S50
Pharmacologic class: Nitrogen Binding Agent; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Standardized Insect Venom Allergenic Extract

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

N459469030110 followed by a unit qualifier and the quantity

Package 59469-0301-10. 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 Jan 11, 2023.

Indications (excerpt from the label)

Indications For relief of minor urinary tract pain. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59469-301

What is NDC 59469-301?: 59469-301 is the product NDC for Akutur, Benzoic acid 4 [hp_X]/50mL + 7 more ingredients solution/ drops, listed with the FDA by PEKANA Nautrheilmittel GmbH. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Akutur (BENZOIC ACID, NITRIC ACID, Apis mellifera, Lytta vesicatoria, Populus tremuloides Bark, ANEMONE PRATENSIS Flowering TOP, GINGER, and Solidago virgaurea Flowering Top).
What is the active ingredient?: Benzoic acid, Nitric acid, Apis mellifera, Lytta vesicatoria, Populus tremuloides bark, Pulsatilla pratensis flowering top, Ginger, Solidago virgaurea flowering top.
Who is the labeler?: PEKANA Nautrheilmittel GmbH, NDC labeler code 59469. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Akutur?: 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.