What is NDC 44911-0279?

44911-0279 is the product NDC for Gynestat, Black cohosh 3 [hp_X]/mL + 10 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?

Gynestat (Cimicifuga Racemosa, Eucalyptus Globulus, Argentum Nitricum, Calcarea Carbonica, Kali Bichromicum, Kreosotum, Mercurius Solubilis, Pulsatilla (Pratensis), Sepia, Staphysagria, Thuja Occidentalis).

What is the active ingredient?

Black cohosh, Eucalyptus globulus leaf, Silver nitrate, Oyster shell calcium carbonate, Crude, Potassium dichromate, Wood creosote, Mercurius solubilis, Pulsatilla pratensis, Sepia officinalis juice, Delphinium staphisagria seed, Thuja occidentalis leafy twig.

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 Gynestat?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Gynestat NDC 44911-0279 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0279Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0279Add 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
44911-0279-1	4491102790144911027901	30 mL in 1 BOTTLE, DROPPER (44911-0279-1)Marketed from Oct 23, 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): Gynestat
Generic name (nonproprietary): cimicifuga racemosa, eucalyptus globulus, argentum nitricum, calcarea carbonica, kali bichromicum, kreosotum, mercurius solubilis, pulsatilla (pratensis), sepia, staphysagria, thuja occidentalis
Active ingredients: Black cohosh — 3 [hp_X]/mLEucalyptus globulus leaf — 3 [hp_X]/mLSilver nitrate — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLPotassium dichromate — 12 [hp_X]/mLWood creosote — 12 [hp_X]/mLMercurius solubilis — 12 [hp_X]/mLPulsatilla pratensis — 12 [hp_X]/mLSepia officinalis juice — 12 [hp_X]/mLDelphinium staphisagria seed — 12 [hp_X]/mLThuja occidentalis leafy twig — 12 [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: Oct 23, 2015
Marketing end: Apr 6, 2028
Identifiers: Product ID 44911-0279_2df8896c-9511-4570-968f-ea020dd3de00SPL ID 2df8896c-9511-4570-968f-ea020dd3de00SPL set ID fb712113-47b5-4e23-aab0-e3242f8655e5UNII K73E24S6X9, S546YLW6E6, 95IT3W8JZE, 2E32821G6I, T4423S18FM, 3JYG22FD73, 324Y4038G2, 8E272251DI, QDL83WN8C2, 00543AP1JV, 1NT28V9397UPC 0363113701159

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

N444911027901 followed by a unit qualifier and the quantity

Package 44911-0279-01. 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 Aug 2, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve menstrual pain and vaginal irritation.** **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)

About NDC 44911-0279

What is NDC 44911-0279?: 44911-0279 is the product NDC for Gynestat, Black cohosh 3 [hp_X]/mL + 10 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?: Gynestat (Cimicifuga Racemosa, Eucalyptus Globulus, Argentum Nitricum, Calcarea Carbonica, Kali Bichromicum, Kreosotum, Mercurius Solubilis, Pulsatilla (Pratensis), Sepia, Staphysagria, Thuja Occidentalis).
What is the active ingredient?: Black cohosh, Eucalyptus globulus leaf, Silver nitrate, Oyster shell calcium carbonate, Crude, Potassium dichromate, Wood creosote, Mercurius solubilis, Pulsatilla pratensis, Sepia officinalis juice, Delphinium staphisagria seed, Thuja occidentalis leafy twig.
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 Gynestat?: 1 other product NDC are listed under this name. See all Gynestat 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 Gynestat NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Gynestatcimicifuga racemosa, eucalyptus globulus, argentum nitricum, aurum muriaticum natronatum, borax, calcarea carbonica, kali bichromicum, kreosotum, lilium tigrinum, mercurius solubilis, pulsatilla (pratensis), sepia, staphysagria, thuja occidentalis	Black cohosh 3 [hp_X]/mL + 13 more ingredients	LiquidOral	Energique, Inc.	44911-0716	44911-0716-01