Lgb HP NDC 43857-0045

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0045Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0045Add 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
43857-0045-1	43857004501	30 mL in 1 BOTTLE, DROPPER (43857-0045-1)Marketed from Jan 18, 2017

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): Lgb HPSuffix: HP
Generic name (nonproprietary): belladonna, chelidonium majus, colocynthis, lycopodium clavatum, natrum sulphuricum, nux vomica, phosphorus, pulsatilla (vulgaris), veratrum album
Active ingredients: Atropa belladonna whole — 30 [hp_X]/mLChelidonium majus whole — 30 [hp_X]/mLCitrullus colocynthis fruit pulp — 30 [hp_X]/mLLycopodium clavatum spore — 30 [hp_X]/mLSodium sulfate — 30 [hp_X]/mLStrychnos nux-vomica seed — 30 [hp_X]/mLPhosphorus — 30 [hp_X]/mLPulsatilla vulgaris whole — 30 [hp_X]/mLVeratrum album root — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 23, 2013
Listing expires: Dec 31, 2027
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 43857-0045_42bdb123-8344-473b-b6b2-4632a1f2e7ecSPL ID 42bdb123-8344-473b-b6b2-4632a1f2e7ecSPL set ID 4f6db767-4c5d-4f86-894d-99ff6db7c920UNII DSV74G1P2J, 7E889U5RNN, 23H32AOH17, C88X29Y479, 0YPR65R21J, 269XH13919, 27YLU75U4W, I76KB35JEV, QNS6W5US1ZUPC 0210184341725
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

N443857004501 followed by a unit qualifier and the quantity

Package 43857-0045-01. 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 Apr 17, 2026.

Indications (excerpt from the label)

USES: For temporary relief of symptoms of complaints of the liver and gall bladder, flatulence, and constipation.** **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)