What is NDC 43857-0610?

43857-0610 is the product NDC for Dv HP, Oyster shell calcium carbonate, Crude 30 [hp_X]/mL + 7 more ingredients liquid, listed with the FDA by BioActive Nutritional, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Dv HP (Calcarea carbonica, Chenopodium anthelminticum, Cocculus indicus, Conium maculatum, Nux vomica, Phosphorus, Pulsatilla (Vulgaris), Silicea).

What is the active ingredient?

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

BioActive Nutritional, Inc., NDC labeler code 43857. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Dv HP?

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.

Dv HP NDC 43857-0610 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0610Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0610Add 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
43857-0610-1	43857061001	30 mL in 1 BOTTLE, DROPPER (43857-0610-1)Marketed from Jun 3, 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): Dv HP
Generic name (nonproprietary): calcarea carbonica, chenopodium anthelminticum, cocculus indicus, conium maculatum, nux vomica, phosphorus, pulsatilla (vulgaris), silicea
Active ingredients: Oyster shell calcium carbonate, Crude — 30 [hp_X]/mLDysphania ambrosioides whole — 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 whole — 30 [hp_X]/mLSilicon dioxide — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.NDC labeler code 43857
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 3, 2021
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 43857-0610_03ded7c3-432a-465e-aaca-42988ff959a4SPL ID 03ded7c3-432a-465e-aaca-42988ff959a4SPL set ID 74bda12d-5e3d-4f52-9e3f-98012c92fc91UNII 2E32821G6I, 4H5RSU087I, 810258W28U, Q28R5GF371, 269XH13919, 27YLU75U4W, I76KB35JEV, ETJ7Z6XBU4
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

N443857061001 followed by a unit qualifier and the quantity

Package 43857-0610-01. 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 Jan 5, 2024.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of symptoms due to dizziness and light-headedness.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43857-0610

What is NDC 43857-0610?: 43857-0610 is the product NDC for Dv HP, Oyster shell calcium carbonate, Crude 30 [hp_X]/mL + 7 more ingredients liquid, listed with the FDA by BioActive Nutritional, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Dv HP (Calcarea carbonica, Chenopodium anthelminticum, Cocculus indicus, Conium maculatum, Nux vomica, Phosphorus, Pulsatilla (Vulgaris), Silicea).
What is the active ingredient?: Oyster shell calcium carbonate, Crude, Dysphania ambrosioides whole, Anamirta cocculus seed, Conium maculatum flowering top, Strychnos nux-vomica seed, Phosphorus, Pulsatilla vulgaris whole, Silicon dioxide.
Who is the labeler?: BioActive Nutritional, Inc., NDC labeler code 43857. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Dv HP?: 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.