Endoplex F NDC 43857-0417

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0417Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0417Add 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
43857-0417-1	43857041701	30 mL in 1 BOTTLE, DROPPER (43857-0417-1)Marketed from Sep 29, 2016

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): Endoplex F
Generic name (nonproprietary): cimicifuga racemosa, fucus vesiculosus, glycyrrhiza glabra, xanthoxylum fraxineum, adrenalinum, cerebrum suis, hypophysis suis, hypothalamus (suis), oophorinum (suis), pineal (suis), thyroidinum (suis), pulsatilla (vulgaris), sepia
Active ingredients: Black cohosh — 3 [hp_X]/mLFucus vesiculosus — 3 [hp_X]/mLGlycyrrhiza glabra — 3 [hp_X]/mLZanthoxylum americanum bark — 3 [hp_X]/mLEpinephrine — 8 [hp_X]/mLSus scrofa cerebrum — 8 [hp_X]/mLSus scrofa pituitary gland, Posterior — 8 [hp_X]/mLSus scrofa hypothalamus — 8 [hp_X]/mLSus scrofa ovary — 8 [hp_X]/mLSus scrofa pineal gland — 8 [hp_X]/mLThyroid — 8 [hp_X]/mLPulsatilla vulgaris whole — 12 [hp_X]/mLSepia officinalis juice — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 29, 2016
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic alpha-Agonists (Mechanism)Adrenergic beta-Agonists (Mechanism)Allergens (Chemical structure)Catecholamines (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 43857-0417_83714b9e-4b13-436f-b1c2-f4575cbb81d2SPL ID 83714b9e-4b13-436f-b1c2-f4575cbb81d2SPL set ID bfe6d42a-a3e5-44b3-ab8f-b08ad4e2b66fUNII K73E24S6X9, 535G2ABX9M, 2788Z9758H, A4KL1HMZ7T, YKH834O4BH, 4GB5DQR532, E8S87O660T, N6R0856Z79, S7YTV04R8O, 050QZ2EDK7, 6RV024OAUQ, I76KB35JEV, QDL83WN8C2UPC 0210184341398
Pharmacologic class: Catecholamine; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; alpha-Adrenergic Agonist; beta-Adrenergic Agonist

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

N443857041701 followed by a unit qualifier and the quantity

Package 43857-0417-01. 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 Mar 30, 2026.

Indications (excerpt from the label)

USES: For temporary relief of menstrual pain and cramps; pain immediately prior to menses, sore tender breasts associated with menstruation.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)