Guna-Pms NDC 17089-290

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-290Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0290Add 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
17089-290-18	17089029018	1 BOTTLE, DROPPER in 1 BOX (17089-290-18) / 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-Pms
Generic name (nonproprietary): arsenic trioxide - estradiol - goldenseal - lachesis muta venom - magnesium phosphate - matricaria recutita - melatonin - progesterone - strychnos nux-vomica seed - sulfur - sus scrofa ovary - sus scrofa pituitary gland -
Active ingredients: Arsenic trioxide — 6 [hp_C]/30mLEstradiol — 6 [hp_X]/30mLGoldenseal — 6 [hp_C]/30mLLachesis muta venom — 4 [hp_C]/30mLMagnesium phosphate, Tribasic, Pentahydrate — 6 [hp_C]/30mLMatricaria recutita — 6 [hp_C]/30mLMelatonin — 4 [hp_C]/30mLProgesterone — 6 [hp_X]/30mLStrychnos nux-vomica seed — 6 [hp_C]/30mLSulfur — 6 [hp_C]/30mLSus scrofa ovary — 8 [hp_X]/30mLSus scrofa pituitary gland — 8 [hp_X]/30mL
Dosage form: Solution/ drops
Route: Oral
Labeler: Guna spa
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 23, 2006
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Estradiol Congeners (Chemical structure)Estrogen Receptor Agonists (Mechanism)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Plant Proteins (Chemical structure)Progesterone (Chemical structure)Seed Storage Proteins (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 17089-290_7e9133b3-3360-2bd0-e053-2a91aa0a3bf3SPL ID 7e9133b3-3360-2bd0-e053-2a91aa0a3bf3SPL set ID 86f341b1-a8f7-4833-a1be-e51610b05bcdUNII S7V92P67HO, 4TI98Z838E, ZW3Z11D0JV, VSW71SS07I, 453COF7817, G0R4UBI2ZZ, JL5DK93RCL, 4G7DS2Q64Y, 269XH13919, 70FD1KFU70, S7YTV04R8O, L0PFEMQ1DTUPC 0317089290186
Pharmacologic class: Calculi Dissolution Agent; Estrogen; Non-Standardized Plant Allergenic Extract; Osmotic Laxative; Progesterone

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

N417089029018 followed by a unit qualifier and the quantity

Package 17089-0290-18. 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)