NDC codes

FDA NDC Directory
Product NDC (as listed)59469-315Labeler and product segments. Claims need a package NDC.
Product NDC at billing width59469-0315Add 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 NDC11-digit (billing)PackageCopy
59469-315-1059469031510594690315101 BOTTLE, GLASS in 1 BOX (59469-315-10) / 50 mL in 1 BOTTLE, GLASSMarketed from Jun 24, 2019
59469-315-4059469031540594690315401 BOTTLE, GLASS in 1 BOX (59469-315-40) / 100 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)
Renelix
Generic name (nonproprietary)
benzoic acid, nitric acid, apis mellifera, berberis vulgaris root bark, colchicum autumnale bulb, protortonia cacti, solidago virgaurea flowering top, and capsella bursa-pastoris top
Active ingredients
Benzoic acid — 4 [hp_X]/50mLNitric acid — 6 [hp_X]/50mLApis mellifera — 4 [hp_X]/50mLBerberis vulgaris root bark — 3 [hp_X]/50mLColchicum autumnale bulb — 12 [hp_X]/50mLProtortonia cacti — 631 mg/50mLSolidago virgaurea flowering top — 2913 mg/50mLCapsella bursa-pastoris top — 510 mg/50mL
Dosage form
Solution/ drops
Route
Oral
Labeler
PEKANA Naturheilmittel GmbHNDC labeler code 59469
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Allergens (Chemical structure)Ammonium Ion Binding Activity (Mechanism)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers
Product ID 59469-315_8ddbd870-0a08-4be8-8d59-b56c164cd02fSPL ID 8ddbd870-0a08-4be8-8d59-b56c164cd02fSPL set ID 11a057e9-4b2a-4de0-a7e9-fbd4029bb7a8UNII 8SKN0B0MIM, 411VRN1TV4, 7S82P3R43Z, 1TH8Q20J0U, 993QHL78E6, LZB7TFX1LT, 5405K23S50, 7D8DU3293G
Pharmacologic class
Nitrogen Binding Agent; 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

N459469031510 followed by a unit qualifier and the quantity

Package 59469-0315-10. 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 .

Indications (excerpt from the label)

Indications Helps cleanse and detoxify the body. 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 59469-315

What is NDC 59469-315?
59469-315 is the product NDC for Renelix, Benzoic acid 4 [hp_X]/50mL + 7 more ingredients solution/ drops, listed with the FDA by PEKANA Naturheilmittel GmbH. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Renelix (Benzoic Acid, Nitric Acid, Apis mellifera, Berberis Vulgaris Root Bark, Colchicum autumnale Bulb, Protortonia Cacti, Solidago virgaurea Flowering Top, and Capsella bursa-pastoris Top).
What is the active ingredient?
Benzoic acid, Nitric acid, Apis mellifera, Berberis vulgaris root bark, Colchicum autumnale bulb, Protortonia cacti, Solidago virgaurea flowering top, Capsella bursa-pastoris top.
Who is the labeler?
PEKANA Naturheilmittel 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 Renelix?
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.

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