What is NDC 43857-0572?

43857-0572 is the product NDC for Albuforce, Equisetum hyemale whole 3 [hp_X]/mL + 6 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?

Albuforce (Equisetum Hyemale, Solidago Virgaurea, Apis Mellifica, Mercurius Corrosivus, Nux Moschata, Phosphorus, Terebinthina).

What is the active ingredient?

Equisetum hyemale whole, Solidago virgaurea flowering top, Apis mellifera, Mercuric chloride, Nutmeg, Phosphorus, Turpentine oil.

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 Albuforce?

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.

Albuforce NDC 43857-0572 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0572Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0572Add 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
43857-0572-1	4385705720143857057201	30 mL in 1 BOTTLE, DROPPER (43857-0572-1)Marketed from Feb 22, 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): Albuforce
Generic name (nonproprietary): equisetum hyemale, solidago virgaurea, apis mellifica, mercurius corrosivus, nux moschata, phosphorus, terebinthina
Active ingredients: Equisetum hyemale whole — 3 [hp_X]/mLSolidago virgaurea flowering top — 3 [hp_X]/mLApis mellifera — 12 [hp_X]/mLMercuric chloride — 12 [hp_X]/mLNutmeg — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLTurpentine oil — 12 [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: Feb 22, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 43857-0572_8b8cd3bb-1bc6-4088-ae5d-0a9eddce3043SPL ID 8b8cd3bb-1bc6-4088-ae5d-0a9eddce3043SPL set ID dca03511-30a1-44f0-a9e1-8e6be1831aa4UNII 59677RXH25, 5405K23S50, 7S82P3R43Z, 53GH7MZT1R, AEE24M3MQ9, 27YLU75U4W, C5H0QJ6V7FUPC 0810184340232
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Standardized Insect Venom 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

N443857057201 followed by a unit qualifier and the quantity

Package 43857-0572-01. 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 May 19, 2025.

Indications (excerpt from the label)

USES: For temporary relief of minor burning and soreness upon urination, mild pain in the region of the right kidney, swelling of the legs, and scanty urination.** **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 43857-0572

What is NDC 43857-0572?: 43857-0572 is the product NDC for Albuforce, Equisetum hyemale whole 3 [hp_X]/mL + 6 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?: Albuforce (Equisetum Hyemale, Solidago Virgaurea, Apis Mellifica, Mercurius Corrosivus, Nux Moschata, Phosphorus, Terebinthina).
What is the active ingredient?: Equisetum hyemale whole, Solidago virgaurea flowering top, Apis mellifera, Mercuric chloride, Nutmeg, Phosphorus, Turpentine oil.
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 Albuforce?: 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.