What is NDC 43857-0340?

43857-0340 is the product NDC for Renaforce, Berberis vulgaris root bark 3 [hp_X]/mL + 5 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?

Renaforce (Berberis Vulgaris, Echinacea (Angustifolia), Coccus Cacti, Kali Muriaticum, Lycopodium Clavatum, Nitricum Acidum).

What is the active ingredient?

Berberis vulgaris root bark, Echinacea angustifolia whole, Protortonia cacti, Potassium chloride, Lycopodium clavatum spore, Nitric acid.

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 Renaforce?

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.

Renaforce NDC 43857-0340 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0340Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0340Add 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
43857-0340-1	4385703400143857034001	30 mL in 1 BOTTLE, DROPPER (43857-0340-1)Marketed from Dec 6, 2016

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): Renaforce
Generic name (nonproprietary): berberis vulgaris, echinacea (angustifolia), coccus cacti, kali muriaticum, lycopodium clavatum, nitricum acidum
Active ingredients: Berberis vulgaris root bark — 3 [hp_X]/mLEchinacea angustifolia whole — 3 [hp_X]/mLProtortonia cacti — 12 [hp_X]/mLPotassium chloride — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLNitric acid — 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: Oct 15, 2014
Listing expires: Dec 31, 2027
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers: Product ID 43857-0340_5b590753-cd51-487e-ad66-90558a3f03faSPL ID 5b590753-cd51-487e-ad66-90558a3f03faSPL set ID 804b7055-e1e6-448d-8257-c562b971f437UNII 1TH8Q20J0U, VB06AV5US8, LZB7TFX1LT, 660YQ98I10, C88X29Y479, 411VRN1TV4UPC 0210184341220
Pharmacologic class: 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

N443857034001 followed by a unit qualifier and the quantity

Package 43857-0340-01. 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 Mar 9, 2026.

Indications (excerpt from the label)

USES: For temporary relief of urine that's scanty, dark, offensive; pain in the back, sensation as if some urine remained after urinating and pain in the thighs and loins on urinating.** **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 43857-0340

What is NDC 43857-0340?: 43857-0340 is the product NDC for Renaforce, Berberis vulgaris root bark 3 [hp_X]/mL + 5 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?: Renaforce (Berberis Vulgaris, Echinacea (Angustifolia), Coccus Cacti, Kali Muriaticum, Lycopodium Clavatum, Nitricum Acidum).
What is the active ingredient?: Berberis vulgaris root bark, Echinacea angustifolia whole, Protortonia cacti, Potassium chloride, Lycopodium clavatum spore, Nitric acid.
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 Renaforce?: 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.