Gynetox NDC 43857-0565

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0565Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0565Add 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
43857-0565-1	43857056501	30 mL in 1 BOTTLE, DROPPER (43857-0565-1)Marketed from Feb 18, 2021

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Gynetox
Generic name (nonproprietary): angelica archangelica, cimicifuga racemosa, zincum gluconicum, funiculus umbilicalis suis, lymph node (suis), oophorinum (suis), uterus (suis), glandula suprarenalis suis, thyroidinum suis, boricum acidum, kreosotum, mercurius solubilis, pulsatilla (pratensis), sepia, calcarea carbonica, phosphorus, sabina, candida albicans, herpes simplex 1 and 2 nosode, human papilloma nosode
Active ingredients: Angelica archangelica root — 3 [hp_X]/mLBlack cohosh — 3 [hp_X]/mLZinc gluconate — 6 [hp_X]/mLSus scrofa umbilical cord — 8 [hp_X]/mLSus scrofa lymph — 8 [hp_X]/mLSus scrofa ovary — 8 [hp_X]/mLSus scrofa uterus — 8 [hp_X]/mLSus scrofa adrenal gland — 9 [hp_X]/mLThyroid — 9 [hp_X]/mLBoric acid — 12 [hp_X]/mLWood creosote — 12 [hp_X]/mLMercurius solubilis — 12 [hp_X]/mLPulsatilla vulgaris whole — 12 [hp_X]/mLSepia officinalis juice — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 30 [hp_X]/mLPhosphorus — 30 [hp_X]/mLJuniperus sabina leafy twig — 30 [hp_X]/mLCandida albicans — 30 [hp_X]/mLHuman herpesvirus 1 — 30 [hp_X]/mLHuman herpesvirus 2 — 30 [hp_X]/mLHuman papillomavirus — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 18, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Decreased Copper Ion Absorption (Physiologic effect)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 43857-0565_c7448b21-f07a-4e31-ad0f-1db7550a9004SPL ID c7448b21-f07a-4e31-ad0f-1db7550a9004SPL set ID 80a5b1f7-9b6b-4314-91c6-20e6b61a5686UNII DTN01M69SN, K73E24S6X9, U6WSN5SQ1Z, 118OYG6W3H, 33A7VYU29L, S7YTV04R8O, 2595C75F1P, 398IYQ16YV, 6RV024OAUQ, R57ZHV85D4, 3JYG22FD73, 324Y4038G2, I76KB35JEV, QDL83WN8C2, 2E32821G6I, 27YLU75U4W, Z5BEX9K2G1, 4D7G21HDBC, 22G38P19RL, 74J6DNH49U, 23CVL7WF4J
Pharmacologic class: Copper Absorption Inhibitor; Non-Standardized Fungal 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

N443857056501 followed by a unit qualifier and the quantity

Package 43857-0565-01. 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 Oct 17, 2024.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of menstrual pain and vaginal irritation.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)