What is NDC 44911-0187?

44911-0187 is the product NDC for Dizziness HP, Oyster shell calcium carbonate, Crude 30 [hp_X]/mL + 8 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?

Dizziness HP (Calcarea carbonica, Chenopodium anthelminticum, Cocculus indicus, Conium maculatum, Nux vomica, Phosphorus, Pulsatilla (pratensis), Silicea, Tabacum,).

What is the active ingredient?

Oyster shell calcium carbonate, Crude, Dysphania ambrosioides, Anamirta cocculus seed, Conium maculatum flowering top, Strychnos nux-vomica seed, Phosphorus, Pulsatilla pratensis whole, Silicon dioxide, Tobacco leaf.

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 Dizziness HP?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Dizziness HP NDC 44911-0187 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0187Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0187Add 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
44911-0187-1	4491101870144911018701	30 mL in 1 BOTTLE, DROPPER (44911-0187-1)Marketed from Jul 8, 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): Dizziness HPSuffix: HP
Generic name (nonproprietary): calcarea carbonica, chenopodium anthelminticum, cocculus indicus, conium maculatum, nux vomica, phosphorus, pulsatilla (pratensis), silicea, tabacum,
Active ingredients: Oyster shell calcium carbonate, Crude — 30 [hp_X]/mLDysphania ambrosioides — 30 [hp_X]/mLAnamirta cocculus seed — 30 [hp_X]/mLConium maculatum flowering top — 30 [hp_X]/mLStrychnos nux-vomica seed — 30 [hp_X]/mLPhosphorus — 30 [hp_X]/mLPulsatilla pratensis whole — 30 [hp_X]/mLSilicon dioxide — 30 [hp_X]/mLTobacco leaf — 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: Jul 8, 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)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 44911-0187_f02fda13-544f-409a-bb7b-038d49cf4932SPL ID f02fda13-544f-409a-bb7b-038d49cf4932SPL set ID 0bf53ecc-c2ad-40b5-b921-7c10a1b00626UNII 2E32821G6I, 4H5RSU087I, 810258W28U, Q28R5GF371, 269XH13919, 27YLU75U4W, 8E272251DI, ETJ7Z6XBU4, 6YR2608RSU
Pharmacologic class: 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

N444911018701 followed by a unit qualifier and the quantity

Package 44911-0187-01. 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 Nov 19, 2025.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve symptoms of dizziness and light-headedness.** **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 44911-0187

What is NDC 44911-0187?: 44911-0187 is the product NDC for Dizziness HP, Oyster shell calcium carbonate, Crude 30 [hp_X]/mL + 8 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?: Dizziness HP (Calcarea carbonica, Chenopodium anthelminticum, Cocculus indicus, Conium maculatum, Nux vomica, Phosphorus, Pulsatilla (pratensis), Silicea, Tabacum,).
What is the active ingredient?: Oyster shell calcium carbonate, Crude, Dysphania ambrosioides, Anamirta cocculus seed, Conium maculatum flowering top, Strychnos nux-vomica seed, Phosphorus, Pulsatilla pratensis whole, Silicon dioxide, Tobacco leaf.
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 Dizziness HP?: 1 other product NDC are listed under this name. See all Dizziness HP 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 Dizziness HP NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Dizziness HPoyster shell calcium carbonate crude, chenopodium ambrosioides, anamirta cocculus seed, conium maculatum flowering top, strychnos nux-vomica seed, phosphorus, pulsatilla vulgaris, silicon dioxide	Oyster shell calcium carbonate, Crude 30 [hp_X]/mL + 7 more ingredients	LiquidOral	Natural Creations, Inc.	43406-0017	43406-0017-01