Guna-Hypertension NDC 17089-347

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-347Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0347Add 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
17089-347-18	17089034718	1 BOTTLE, DROPPER in 1 BOX (17089-347-18) / 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): Guna-Hypertension
Generic name (nonproprietary): arnica montana - fumaric acid - gold - lead - melatonin - melilotus - olea europaea flower - pork kidney - rauwolfia serpentina - sodium pyruvate - spigelia - sus scrofa adrenal gland - sus scrofa diencephalon - ubidecarenone - viscum album fruit -
Active ingredients: Arnica montana — 12 [hp_X]/30mLGold — 12 [hp_X]/30mLUbidecarenone — 3 [hp_X]/30mLSus scrofa diencephalon — 6 [hp_X]/30mLFumaric acid — 3 [hp_X]/30mLSus scrofa adrenal gland — 200 [hp_X]/30mLPork kidney — 6 [hp_X]/30mLMelatonin — 4 [hp_C]/30mLMelilotus — 6 [hp_X]/30mLSodium pyruvate — 3 [hp_X]/30mLOlea europaea flower — 3 [hp_X]/30mLLead — 12 [hp_X]/30mLRauwolfia serpentina — 6 [hp_X]/30mLSpigelia — 6 [hp_X]/30mLViscum album fruit — 3 [hp_X]/30mL
Dosage form: Solution/ drops
Route: Oral
Labeler: Guna spa
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 16, 2008
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 17089-347_7e02b61a-2014-7b6d-e053-2991aa0abb80SPL ID 7e02b61a-2014-7b6d-e053-2991aa0abb80SPL set ID 40c5b156-dc5c-41c2-88c3-a9bf28119d22UNII O80TY208ZW, 79Y1949PYO, EJ27X76M46, 23PJ4252VL, 88XHZ13131, 398IYQ16YV, X7BCI5P86H, JL5DK93RCL, F22I9R6Q0X, POD38AIF08, 498M34P1VZ, 2P299V784P, H192N84N1G, 467D26HS0B, P83EQ521R3UPC 0317089347187
Pharmacologic class: Standardized Chemical Allergen

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

N417089034718 followed by a unit qualifier and the quantity

Package 17089-0347-18. 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 Dec 21, 2018.

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)