What is NDC 61096-2014?

61096-2014 is the product NDC for MenoPower, Arnica montana whole 200 [hp_C]/41mL + 6 more ingredients liquid, listed with the FDA by Eight and Company L.L.C. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

MenoPower (Arnica, Glonoinum, Lachesis, Oophorinum, Salvia, Sanguinaria, Sepia).

What is the active ingredient?

Arnica montana whole, Nitroglycerin, Lachesis muta venom, Sus scrofa ovary, Sage, Sanguinaria canadensis root, Sepia officinalis juice.

Eight and Company L.L.C, NDC labeler code 61096. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for MenoPower?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

MenoPower NDC 61096-2014 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)61096-2014Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61096-2014Add 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
61096-2014-1	6109620140161096201401	1 BOTTLE, SPRAY in 1 CARTON (61096-2014-1) / 41 mL in 1 BOTTLE, SPRAYMarketed from Mar 12, 2019

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): MenoPower
Generic name (nonproprietary): arnica, glonoinum, lachesis, oophorinum, salvia, sanguinaria, sepia
Active ingredients: Arnica montana whole — 200 [hp_C]/41mLNitroglycerin — 200 [hp_C]/41mLLachesis muta venom — 200 [hp_C]/41mLSus scrofa ovary — 30 [hp_C]/41mLSage — 4 [hp_X]/41mLSanguinaria canadensis root — 200 [hp_C]/41mLSepia officinalis juice — 200 [hp_C]/41mL
Dosage form: Liquid
Route: Oral
Labeler: Eight and Company L.L.CNDC labeler code 61096
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 8, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Nitrates (Chemical structure)Plant Proteins (Chemical structure)Vasodilation (Physiologic effect)
Identifiers: Product ID 61096-2014_8fdce44b-8097-4a66-85ec-139d23f0f264SPL ID 8fdce44b-8097-4a66-85ec-139d23f0f264SPL set ID 1e1e79fe-fa8f-4e05-bcff-3a792eb63b35UNII O80TY208ZW, G59M7S0WS3, VSW71SS07I, S7YTV04R8O, 065C5D077J, N9288CD508, QDL83WN8C2
Pharmacologic class: Nitrate Vasodilator; Non-Standardized Food 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

N461096201401 followed by a unit qualifier and the quantity

Package 61096-2014-01. 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 18, 2025.

Indications (excerpt from the label)

INDICATIONS: Temporarily relieves common menopausal symptoms associated with hormonal imbalances, including: ° emotional fluctuations ° hot flashes and night sweats ° irritability ° vaginal dryness ° natural ° gluten & lactose free ° no artificial flavors or colors ° no known negative side effects ° no known negative drug interactions

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 61096-2014

What is NDC 61096-2014?: 61096-2014 is the product NDC for MenoPower, Arnica montana whole 200 [hp_C]/41mL + 6 more ingredients liquid, listed with the FDA by Eight and Company L.L.C. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: MenoPower (Arnica, Glonoinum, Lachesis, Oophorinum, Salvia, Sanguinaria, Sepia).
What is the active ingredient?: Arnica montana whole, Nitroglycerin, Lachesis muta venom, Sus scrofa ovary, Sage, Sanguinaria canadensis root, Sepia officinalis juice.
Who is the labeler?: Eight and Company L.L.C, NDC labeler code 61096. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for MenoPower?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.