Ovaplex NDC 43857-0204

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0204Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0204Add 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
43857-0204-1	43857020401	30 mL in 1 BOTTLE, DROPPER (43857-0204-1)Marketed from Aug 21, 2013

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): Ovaplex
Generic name (nonproprietary): angelica archangelica, caulophyllum thalictroides, dioscorea villosa, hypophysis suis, oophorinum (suis) thyroidinum (suis), uterus suis, zincum gluconicum, apis mellifica, belladonna, cimicifuga racemosa, magnesia phosphorica, sepia
Active ingredients: Angelica archangelica root — 3 [hp_X]/mLCaulophyllum thalictroides root — 3 [hp_X]/mLDioscorea villosa tuber — 3 [hp_X]/mLSus scrofa ovary — 6 [hp_X]/mLSus scrofa pituitary gland — 6 [hp_X]/mLThyroid — 6 [hp_X]/mLSus scrofa uterus — 6 [hp_X]/mLZinc gluconate — 6 [hp_X]/mLApis mellifera — 12 [hp_X]/mLAtropa belladonna — 12 [hp_X]/mLBlack cohosh — 12 [hp_X]/mLMagnesium phosphate, Dibasic trihydrate — 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: Aug 21, 2013
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Decreased Copper Ion Absorption (Physiologic effect)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)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 43857-0204_695947b4-90e2-4f57-bc17-5eba346c0c71SPL ID 695947b4-90e2-4f57-bc17-5eba346c0c71SPL set ID cdbc8dc0-ac22-46af-a516-a3b5ca358197UNII DTN01M69SN, JTJ6HH6YEH, IWY3IWX2G8, S7YTV04R8O, L0PFEMQ1DT, 6RV024OAUQ, 2595C75F1P, U6WSN5SQ1Z, 7S82P3R43Z, WQZ3G9PF0H, K73E24S6X9, HF539G9L3Q, QDL83WN8C2UPC 0810184340171
Pharmacologic class: Calculi Dissolution Agent; Copper Absorption Inhibitor; Osmotic Laxative; Standardized Insect Venom 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

N443857020401 followed by a unit qualifier and the quantity

Package 43857-0204-01. 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 Apr 2, 2025.

Indications (excerpt from the label)

USES: For temporary relief of painful menses and menstrual cramps.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)