What is NDC 43857-0645?

43857-0645 is the product NDC for Epiforce P, Baptisia tinctoria root 3 [hp_X]/mL + 19 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?

Epiforce P (Baptisia Tinctoria, Berberis Vulgaris, Echinacea (Angustifolia), Glycyrrhiza Glabra, Lappa Major, Rhamnus Frangula, Rhamnus Purshiana, Trifolium Pratense, Xanthoxylum Fraxineum, Phytolacca Decandra, Hydrastis Canadensis, Arsenicum Iodatum, Calcarea Carbonica, Clematis Erecta, Graphites, Kali Muriaticum, Kali Sulphuricum, Mezereum Petroleum, Sepia).

What is the active ingredient?

Baptisia tinctoria root, Berberis vulgaris root bark, Echinacea angustifolia whole, Glycyrrhiza glabra, Arctium lappa root, Frangula alnus bark, Frangula purshiana bark, Trifolium pratense flower, Zanthoxylum americanum bark, Phytolacca americana root, Goldenseal, Arsenic triiodide, Oyster shell calcium carbonate, Crude, Clematis recta flowering top, Graphite, Potassium chloride, Potassium sulfate, Daphne mezereum bark, Kerosene, Sepia officinalis juice.

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 Epiforce P?

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.

Epiforce P NDC 43857-0645 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0645Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0645Add 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
43857-0645-1	4385706450143857064501	30 mL in 1 BOTTLE, DROPPER (43857-0645-1)Marketed from Dec 12, 2024

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): Epiforce P
Generic name (nonproprietary): baptisia tinctoria, berberis vulgaris, echinacea (angustifolia), glycyrrhiza glabra, lappa major, rhamnus frangula, rhamnus purshiana, trifolium pratense, xanthoxylum fraxineum, phytolacca decandra, hydrastis canadensis, arsenicum iodatum, calcarea carbonica, clematis erecta, graphites, kali muriaticum, kali sulphuricum, mezereum petroleum, sepia
Active ingredients: Baptisia tinctoria root — 3 [hp_X]/mLBerberis vulgaris root bark — 3 [hp_X]/mLEchinacea angustifolia whole — 3 [hp_X]/mLGlycyrrhiza glabra — 3 [hp_X]/mLArctium lappa root — 3 [hp_X]/mLFrangula alnus bark — 3 [hp_X]/mLFrangula purshiana bark — 3 [hp_X]/mLTrifolium pratense flower — 3 [hp_X]/mLZanthoxylum americanum bark — 3 [hp_X]/mLPhytolacca americana root — 4 [hp_X]/mLGoldenseal — 5 [hp_Q]/mLArsenic triiodide — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLClematis recta flowering top — 12 [hp_X]/mLGraphite — 12 [hp_X]/mLPotassium chloride — 12 [hp_X]/mLPotassium sulfate — 12 [hp_X]/mLDaphne mezereum bark — 12 [hp_X]/mLKerosene — 12 [hp_X]/mLSepia officinalis juice — 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: Dec 12, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Plant Proteins (Chemical structure)Potassium Compounds (Chemical structure)Potassium Compounds (Chemical structure)
Identifiers: Product ID 43857-0645_f7bbfab2-45d8-4e99-9d42-685a6d15050fSPL ID f7bbfab2-45d8-4e99-9d42-685a6d15050fSPL set ID d33282bf-2045-4b92-a377-013fa711c877UNII 5EF0HWI5WU, 1TH8Q20J0U, VB06AV5US8, 2788Z9758H, 597E9BI3Z3, S2D77IH61R, 4VBP01X99F, 4JS0838828, A4KL1HMZ7T, 11E6VI8VEG, ZW3Z11D0JV, 3029988O2T, 2E32821G6I, 396421SP9F, 4QQN74LH4O, 660YQ98I10, 1K573LC5TV, X2N6E405GV, 1C89KKC04E, QDL83WN8C2
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Osmotic Laxative; Potassium Salt

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

N443857064501 followed by a unit qualifier and the quantity

Package 43857-0645-01. 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 12, 2024.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of unhealthy irritated or broken skin, itching, burning, swelling of skin, dry ro9ugh, scaly skin and eruptions on scalp and bends of joints with itching.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43857-0645

What is NDC 43857-0645?: 43857-0645 is the product NDC for Epiforce P, Baptisia tinctoria root 3 [hp_X]/mL + 19 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?: Epiforce P (Baptisia Tinctoria, Berberis Vulgaris, Echinacea (Angustifolia), Glycyrrhiza Glabra, Lappa Major, Rhamnus Frangula, Rhamnus Purshiana, Trifolium Pratense, Xanthoxylum Fraxineum, Phytolacca Decandra, Hydrastis Canadensis, Arsenicum Iodatum, Calcarea Carbonica, Clematis Erecta, Graphites, Kali Muriaticum, Kali Sulphuricum, Mezereum Petroleum, Sepia).
What is the active ingredient?: Baptisia tinctoria root, Berberis vulgaris root bark, Echinacea angustifolia whole, Glycyrrhiza glabra, Arctium lappa root, Frangula alnus bark, Frangula purshiana bark, Trifolium pratense flower, Zanthoxylum americanum bark, Phytolacca americana root, Goldenseal, Arsenic triiodide, Oyster shell calcium carbonate, Crude, Clematis recta flowering top, Graphite, Potassium chloride, Potassium sulfate, Daphne mezereum bark, Kerosene, Sepia officinalis juice.
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 Epiforce P?: 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.