What is NDC 43406-0017?

43406-0017 is the product NDC for Dizziness HP, Oyster shell calcium carbonate, Crude 30 [hp_X]/mL + 7 more ingredients liquid, listed with the FDA by Natural Creations, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Dizziness HP (Oyster Shell Calcium Carbonate Crude, Chenopodium Ambrosioides, Anamirta Cocculus Seed, Conium Maculatum Flowering Top, Strychnos Nux-Vomica Seed, Phosphorus, Pulsatilla Vulgaris, Silicon Dioxide).

What is the active ingredient?

Oyster shell calcium carbonate, Crude, Chenopodium ambrosioides, Anamirta cocculus seed, Conium maculatum flowering top, Strychnos nux-vomica seed, Phosphorus, Pulsatilla vulgaris, Silicon dioxide.

Natural Creations, Inc., NDC labeler code 43406. 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 43406-0017 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43406-0017Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43406-0017Add 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
43406-0017-1	4340600170143406001701	30 mL in 1 BOTTLE, DROPPER (43406-0017-1)Marketed from May 29, 2007

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 HP
Generic name (nonproprietary): oyster shell calcium carbonate crude, chenopodium ambrosioides, anamirta cocculus seed, conium maculatum flowering top, strychnos nux-vomica seed, phosphorus, pulsatilla vulgaris, silicon dioxide
Active ingredients: Oyster shell calcium carbonate, Crude — 30 [hp_X]/mLChenopodium 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 vulgaris — 30 [hp_X]/mLSilicon dioxide — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Natural Creations, Inc.NDC labeler code 43406
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 29, 2007
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 43406-0017_05fb4634-169b-4384-9c7a-a5e3da911e1bSPL ID 05fb4634-169b-4384-9c7a-a5e3da911e1bSPL set ID 9701096b-5efa-4acd-9227-339ecedfd672UNII 2E32821G6I, 4H5RSU087I, 810258W28U, Q28R5GF371, 269XH13919, 27YLU75U4W, I76KB35JEV, ETJ7Z6XBU4UPC 0877730001245
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

N443406001701 followed by a unit qualifier and the quantity

Package 43406-0017-01. 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 10, 2025.

Indications (excerpt from the label)

USES: Temporarily relieves dizziness and nausea.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43406-0017

What is NDC 43406-0017?: 43406-0017 is the product NDC for Dizziness HP, Oyster shell calcium carbonate, Crude 30 [hp_X]/mL + 7 more ingredients liquid, listed with the FDA by Natural Creations, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Dizziness HP (Oyster Shell Calcium Carbonate Crude, Chenopodium Ambrosioides, Anamirta Cocculus Seed, Conium Maculatum Flowering Top, Strychnos Nux-Vomica Seed, Phosphorus, Pulsatilla Vulgaris, Silicon Dioxide).
What is the active ingredient?: Oyster shell calcium carbonate, Crude, Chenopodium ambrosioides, Anamirta cocculus seed, Conium maculatum flowering top, Strychnos nux-vomica seed, Phosphorus, Pulsatilla vulgaris, Silicon dioxide.
Who is the labeler?: Natural Creations, Inc., NDC labeler code 43406. 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 HPcalcarea carbonica, chenopodium anthelminticum, cocculus indicus, conium maculatum, nux vomica, phosphorus, pulsatilla (pratensis), silicea, tabacum,	Oyster shell calcium carbonate, Crude 30 [hp_X]/mL + 8 more ingredients	LiquidOral	Energique, Inc.	44911-0187	44911-0187-01