Guna Female Support NDC 17089-501

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-501Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0501Add 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
17089-501-18	17089050118	1 BOTTLE, DROPPER in 1 BOX (17089-501-18) / 30 mL in 1 BOTTLE, DROPPERMarketed from Feb 17, 2021

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 Female Support
Generic name (nonproprietary): lilium lancifolium whole flowering - sus scrofa ovary - sus scrofa pituitary gland - sepia officinalis juice - adenosine cyclic phosphate - pulsatilla vulgaris - sus scrofa hypothalamus - sus scrofa adrenal gland - sus scrofa pancreas - magnesium phosphate dibasic trihydrate
Active ingredients: Lilium lancifolium whole flowering — 6 [hp_X]/30mLSus scrofa ovary — 6 [hp_X]/30mLSepia officinalis juice — 10 [hp_X]/30mLAdenosine cyclic phosphate — 6 [hp_X]/30mLSus scrofa pituitary gland — 30 [hp_X]/30mLSus scrofa hypothalamus — 30 [hp_X]/30mLSus scrofa adrenal gland — 30 [hp_X]/30mLSus scrofa pancreas — 30 [hp_X]/30mLMagnesium phosphate, Dibasic trihydrate — 10 [hp_X]/30mLPulsatilla vulgaris — 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: Feb 17, 2021
Listing expires: Dec 31, 2026
Other FDA classes: 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)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 17089-501_bb2217fc-c752-20b1-e053-2995a90a2562SPL ID bb2217fc-c752-20b1-e053-2995a90a2562SPL set ID bb22182f-a503-433f-e053-2995a90a2f47UNII X67Z2963PI, S7YTV04R8O, QDL83WN8C2, E0399OZS9N, L0PFEMQ1DT, N6R0856Z79, 398IYQ16YV, 9Y3J3362RY, HF539G9L3Q, I76KB35JEVUPC 0317089501183
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative

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

N417089050118 followed by a unit qualifier and the quantity

Package 17089-0501-18. 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 Feb 12, 2021.

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)