Rhustoxoforce NDC 43857-0206

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0206Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0206Add 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
43857-0206-1	43857020601	30 mL in 1 BOTTLE, DROPPER (43857-0206-1)Marketed from Aug 21, 2013

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): Rhustoxoforce
Generic name (nonproprietary): apis mellifica, cantharis, graphites, natrum muriaticum, rhus glabra, rhus toxicodendron, rhus venenata, urtica dioica
Active ingredients: Apis mellifera — 12 [hp_X]/mLLytta vesicatoria — 12 [hp_X]/mLGraphite — 12 [hp_X]/mLSodium chloride — 12 [hp_X]/mLRhus glabra top — 12 [hp_X]/mLToxicodendron pubescens leaf — 12 [hp_X]/mLToxicodendron vernix leafy twig — 12 [hp_X]/mLUrtica dioica whole — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 21, 2013
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 43857-0206_54b0f27e-8a42-4a42-8a57-ffd42eefbd9eSPL ID 54b0f27e-8a42-4a42-8a57-ffd42eefbd9eSPL set ID 5a3627f1-a850-42f3-8c7a-b2067bd03538UNII 7S82P3R43Z, 3Q034RO3BT, 4QQN74LH4O, 451W47IQ8X, RHH784E0K6, 6IO182RP7A, Y3VW699H96, 710FLW4U46
Pharmacologic class: 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

N443857020601 followed by a unit qualifier and the quantity

Package 43857-0206-01. 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 Oct 18, 2024.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of allergies caused by poison ivy, oak, and summac.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)