NDC codes

FDA NDC Directory
Product NDC (as listed)17089-415Labeler and product segments. Claims need a package NDC.
Product NDC at billing width17089-0415Add 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
17089-415-1817089041518170890415181 BOTTLE, DROPPER in 1 BOX (17089-415-18) / 30 mL in 1 BOTTLE, DROPPERMarketed from Dec 21, 2018

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)
Eubioflor
Generic name (nonproprietary)
activated charcoal - aethusa cynapium - althaea officinalis leaf - bilberry - candida albicans - uncaria tomentosa - escherichia coli - indole - mercurius solubilis - okoubaka aubrevillei bark - pork liver - proteus vulgaris - silybum marianum seed - skatole - strychnos nux-vomica seed - sus scrofa colon - sus scrofa gall bladder - sus scrofa pancreas - tabebuia impetiginosa bark - taraxacum officinale - veratrum album root -
Active ingredients
Okoubaka aubrevillei bark — 6 [hp_X]/30mLSus scrofa pancreas — 12 [hp_X]/30mLTabebuia impetiginosa bark — 4 [hp_X]/30mLProteus vulgaris — 12 [hp_X]/30mLSkatole — 30 [hp_X]/30mLTaraxacum officinale — 4 [hp_X]/30mLBilberry — 4 [hp_X]/30mLVeratrum album root — 6 [hp_X]/30mLMercurius solubilis — 200 [hp_X]/30mLAethusa cynapium — 6 [hp_X]/30mLAlthaea officinalis leaf — 4 [hp_X]/30mLCandida albicans — 30 [hp_X]/30mLActivated charcoal — 6 [hp_X]/30mLSilybum marianum seed — 4 [hp_X]/30mLCat's claw — 4 [hp_X]/30mLEscherichia coli — 30 [hp_X]/30mLSus scrofa colon — 30 [hp_X]/30mLSus scrofa gallbladder — 6 [hp_X]/30mLPork liver — 12 [hp_X]/30mLIndole — 12 [hp_X]/30mLStrychnos nux-vomica seed — 6 [hp_X]/30mL
Dosage form
Solution/ drops
Route
Oral
Labeler
Guna spaNDC labeler code 17089
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers
Product ID 17089-415_53e9feb6-6a01-a425-e063-6394a90ad978SPL ID 53e9feb6-6a01-a425-e063-6394a90ad978SPL set ID 7dacc28a-2185-4566-8e83-c7a70338797fUNII MK2074187Z, 9Y3J3362RY, 6GLA1946WX, 11T9HCO30O, 9W945B5H7R, 39981FM375, 9P2U39H18W, QNS6W5US1Z, 324Y4038G2, M6936L953C, E2QQV92338, 4D7G21HDBC, 2P3VWU3H10, U946SH95EE, 9060PRM18Q, 514B9K0L10, 94J255A0UC, B6A98VOI9I, 6EC706HI7F, 8724FJW4M5, 269XH13919UPC 0317089415183
Pharmacologic class
Non-Standardized Fungal Allergenic Extract; Non-Standardized Plant 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

N417089041518 followed by a unit qualifier and the quantity

Package 17089-0415-18. 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)

Take 15 minutes before meals

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 17089-415

What is NDC 17089-415?
17089-415 is the product NDC for Eubioflor, Okoubaka aubrevillei bark 6 [hp_X]/30mL + 20 more ingredients solution/ drops, listed with the FDA by Guna spa. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Eubioflor (Activated charcoal - aethusa cynapium - althaea officinalis leaf - bilberry - candida albicans - uncaria tomentosa - escherichia coli - indole - mercurius solubilis - okoubaka aubrevillei bark - pork liver - proteus vulgaris - silybum marianum seed - skatole - strychnos nux-vomica seed - sus scrofa colon - sus scrofa gall bladder - sus scrofa pancreas - tabebuia impetiginosa bark - taraxacum officinale - veratrum album root -).
What is the active ingredient?
Okoubaka aubrevillei bark, Sus scrofa pancreas, Tabebuia impetiginosa bark, Proteus vulgaris, Skatole, Taraxacum officinale, Bilberry, Veratrum album root, Mercurius solubilis, Aethusa cynapium, Althaea officinalis leaf, Candida albicans, Activated charcoal, Silybum marianum seed, Cat's claw, Escherichia coli, Sus scrofa colon, Sus scrofa gallbladder, Pork liver, Indole, Strychnos nux-vomica seed.
Who is the labeler?
Guna spa, NDC labeler code 17089. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Eubioflor?
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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