What is NDC 44911-0607?

44911-0607 is the product NDC for Femstat C, Echinacea angustifolia whole 3 [hp_X]/mL + 9 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Femstat C (Echinacea (Angustifolia), Fucus Vesiculosus, Hydrastis Canadensis, Phytolacca Decandra, Kreosotum, Natrum Muriaticum, Candida Albicans, Lycopodium Clavatum, Pulsatilla (Pratensis), Sepia).

What is the active ingredient?

Echinacea angustifolia whole, Fucus vesiculosus, Goldenseal, Phytolacca americana root, Wood creosote, Sodium chloride, Candida albicans, Lycopodium clavatum spore, Pulsatilla pratensis whole, Sepia officinalis juice.

Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Femstat C?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Femstat C NDC 44911-0607 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0607Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0607Add 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
44911-0607-1	4491106070144911060701	30 mL in 1 BOTTLE, DROPPER (44911-0607-1)Marketed from May 26, 2021

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): Femstat C
Generic name (nonproprietary): echinacea (angustifolia), fucus vesiculosus, hydrastis canadensis, phytolacca decandra, kreosotum, natrum muriaticum, candida albicans, lycopodium clavatum, pulsatilla (pratensis), sepia
Active ingredients: Echinacea angustifolia whole — 3 [hp_X]/mLFucus vesiculosus — 3 [hp_X]/mLGoldenseal — 6 [hp_X]/mLPhytolacca americana root — 6 [hp_X]/mLWood creosote — 12 [hp_X]/mLSodium chloride — 12 [hp_X]/mLCandida albicans — 12 [hp_X]/mLLycopodium clavatum spore — 30 [hp_X]/mLPulsatilla pratensis whole — 30 [hp_X]/mLSepia officinalis juice — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.NDC labeler code 44911
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 26, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 44911-0607_b82b0bcb-2279-4e39-ab1b-2316f7d7ca7dSPL ID b82b0bcb-2279-4e39-ab1b-2316f7d7ca7dSPL set ID 2af0dc7b-5f8b-44fa-9589-bc95043428e9UNII VB06AV5US8, 535G2ABX9M, ZW3Z11D0JV, 11E6VI8VEG, 3JYG22FD73, 451W47IQ8X, 4D7G21HDBC, C88X29Y479, 8E272251DI, QDL83WN8C2UPC 0363113700459
Pharmacologic class: Non-Standardized Fungal 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

N444911060701 followed by a unit qualifier and the quantity

Package 44911-0607-01. 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 24, 2024.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of bloating of the stomach, flatulence and rhinitis.** **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)

About NDC 44911-0607

What is NDC 44911-0607?: 44911-0607 is the product NDC for Femstat C, Echinacea angustifolia whole 3 [hp_X]/mL + 9 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Femstat C (Echinacea (Angustifolia), Fucus Vesiculosus, Hydrastis Canadensis, Phytolacca Decandra, Kreosotum, Natrum Muriaticum, Candida Albicans, Lycopodium Clavatum, Pulsatilla (Pratensis), Sepia).
What is the active ingredient?: Echinacea angustifolia whole, Fucus vesiculosus, Goldenseal, Phytolacca americana root, Wood creosote, Sodium chloride, Candida albicans, Lycopodium clavatum spore, Pulsatilla pratensis whole, Sepia officinalis juice.
Who is the labeler?: Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Femstat C?: 1 other product NDC are listed under this name. See all Femstat C NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Femstat C NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Femstat Cechinacea (angustifolia), fucus vesiculosus, hydrastis canadensis, phytolacca decandra, kreosotum, natrum muriaticum, candida albicans, lycopodium clavatum, pulsatilla (pratensis), sepia	Echinacea angustifolia whole 3 [hp_X]/mL + 9 more ingredients	LiquidOral	Energique, Inc.	44911-0606	44911-0606-01