Menopause HP NDC 44911-0248

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0248Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0248Add 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
44911-0248-1	44911024801	30 mL in 1 BOTTLE, DROPPER (44911-0248-1)Marketed from Aug 27, 2015

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 HPSuffix: HP
Generic name (nonproprietary): belladonna, lachesis mutus, manganum aceticum, nux vomica, pulsatilla (pratensis), secale cornutum, sepia, ustilago maidis
Active ingredients: Atropa belladonna — 30 [hp_X]/mLLachesis muta venom — 30 [hp_X]/mLManganese acetate tetrahydrate — 30 [hp_X]/mLStrychnos nux-vomica seed — 30 [hp_X]/mLPulsatilla pratensis 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: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 27, 2015
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)Magnetic Resonance Contrast Activity (Mechanism)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 44911-0248_43f78cc7-08b2-4be9-96fb-8b86e3a840a0SPL ID 43f78cc7-08b2-4be9-96fb-8b86e3a840a0SPL set ID 6412a5f1-5587-4d4e-8d3f-692979415436UNII WQZ3G9PF0H, VSW71SS07I, 9TO51D176N, 269XH13919, 8E272251DI, 01G9XEA93N, QDL83WN8C2, 4K7Z7K7SWG
Pharmacologic class: Non-Standardized Fungal Allergenic Extract; Non-Standardized Plant Allergenic Extract; Paramagnetic Contrast Agent

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

N444911024801 followed by a unit qualifier and the quantity

Package 44911-0248-01. 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 29, 2024.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of symptoms due to autonomic dysregulation, dryness and irritation of the vagina.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)