Menopause HP NDC 43857-0203

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0203Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0203Add 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
43857-0203-1	43857020301	30 mL in 1 BOTTLE, DROPPER (43857-0203-1)Marketed from Apr 6, 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): Menopause HP
Generic name (nonproprietary): belladonna, lachesis mutus, nux vomica, pulsatilla (vulgaris), secale cornutum, sepia, ustilago maidis
Active ingredients: Atropa belladonna — 30 [hp_X]/mLLachesis muta venom — 30 [hp_X]/mLStrychnos nux-vomica seed — 30 [hp_X]/mLPulsatilla vulgaris whole — 30 [hp_X]/mLClaviceps purpurea sclerotium — 30 [hp_X]/mLSepia officinalis juice — 30 [hp_X]/mLUstilago maydis — 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: Sep 11, 2013
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 43857-0203_8900dc93-f5c1-4fd5-b4f9-fd57c92ccc2dSPL ID 8900dc93-f5c1-4fd5-b4f9-fd57c92ccc2dSPL set ID 0f0aea3f-95d2-4a81-8180-cf675eeb7f62UNII WQZ3G9PF0H, VSW71SS07I, 269XH13919, I76KB35JEV, 01G9XEA93N, QDL83WN8C2, 4K7Z7K7SWG
Pharmacologic class: Non-Standardized Fungal Allergenic Extract; Non-Standardized Plant 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

N443857020301 followed by a unit qualifier and the quantity

Package 43857-0203-01. 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 Dec 17, 2025.

Indications (excerpt from the label)

USES: For temporary relief of mood swings, flushes of heat and physical weakness due to menopause.** **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)