What is NDC 43857-0534?

43857-0534 is the product NDC for Universaltox, Alfalfa 3 [hp_X]/mL + 18 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?

Universaltox (Alfalfa, Avena Sativa, Fucus Vesiculosus, Hordeum Vulgare, Nasturtium Aquaticum, Raphanus Sativus, Triticum Aestivum, Iodium, Ubidecarenonum, Glandula Suprarenalis Suis, Hepar Suis, Manganese Gluconate, Oryza Sativa, Thyroidinum (Suis), Calcarea Carbonica, Natrum Muriaticum, Pulsatilla (Pratensis), Rhus Tox, Cortisone Aceticum).

What is the active ingredient?

Alfalfa, Avena sativa flowering top, Fucus vesiculosus, Hordeum vulgare top, Nasturtium officinale, Daikon, Triticum aestivum whole, Iodine, Ubidecarenone, Sus scrofa adrenal gland, Pork liver, Manganese gluconate, Brown rice, Thyroid, Oyster shell calcium carbonate, Crude, Sodium chloride, Pulsatilla pratensis whole, Toxicodendron pubescens leaf, Cortisone acetate.

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 Universaltox?

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.

Universaltox NDC 43857-0534 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0534Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0534Add 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
43857-0534-1	4385705340143857053401	30 mL in 1 BOTTLE, DROPPER (43857-0534-1)Marketed from Oct 3, 2019

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): Universaltox
Generic name (nonproprietary): alfalfa, avena sativa, fucus vesiculosus, hordeum vulgare, nasturtium aquaticum, raphanus sativus, triticum aestivum, iodium, ubidecarenonum, glandula suprarenalis suis, hepar suis, manganese gluconate, oryza sativa, thyroidinum (suis), calcarea carbonica, natrum muriaticum, pulsatilla (pratensis), rhus tox, cortisone aceticum
Active ingredients: Alfalfa — 3 [hp_X]/mLAvena sativa flowering top — 3 [hp_X]/mLFucus vesiculosus — 4 [hp_X]/mLHordeum vulgare top — 4 [hp_X]/mLNasturtium officinale — 4 [hp_X]/mLDaikon — 4 [hp_X]/mLTriticum aestivum whole — 4 [hp_X]/mLIodine — 6 [hp_X]/mLUbidecarenone — 6 [hp_X]/mLSus scrofa adrenal gland — 8 [hp_X]/mLPork liver — 8 [hp_X]/mLManganese gluconate — 8 [hp_X]/mLBrown rice — 8 [hp_X]/mLThyroid — 8 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLSodium chloride — 12 [hp_X]/mLPulsatilla pratensis whole — 12 [hp_X]/mLToxicodendron pubescens leaf — 12 [hp_X]/mLCortisone acetate — 30 [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 3, 2019
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Corticosteroid Hormone Receptor Agonists (Mechanism)Dietary Proteins (Chemical structure)Grain Proteins (EXT)Increased Histamine Release (Physiologic effect)Magnetic Resonance Contrast Activity (Mechanism)
Identifiers: Product ID 43857-0534_029b94bd-3241-4a9b-80f8-29996a8905a8SPL ID 029b94bd-3241-4a9b-80f8-29996a8905a8SPL set ID ad454e8a-4f78-4aac-90d9-a3f26a6fbe42UNII DJO934BRBD, MA9CQJ3F7F, 535G2ABX9M, 86507VZR9K, YH89GMV676, 86R5J6D01D, 3C3Y389JBU, 9679TC07X4, EJ27X76M46, 398IYQ16YV, 6EC706HI7F, 9YY2F980SV, 659G217HPG, 6RV024OAUQ, 2E32821G6I, 451W47IQ8X, 8E272251DI, 6IO182RP7A, 883WKN7W8X
Pharmacologic class: Corticosteroid; Non-Standardized Food Allergenic Extract; Paramagnetic Contrast Agent

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

N443857053401 followed by a unit qualifier and the quantity

Package 43857-0534-01. 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 17, 2026.

Indications (excerpt from the label)

USES: For temporary relief of sinus congestion, dry cough in the evening and rhinitis.** **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 43857-0534

What is NDC 43857-0534?: 43857-0534 is the product NDC for Universaltox, Alfalfa 3 [hp_X]/mL + 18 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?: Universaltox (Alfalfa, Avena Sativa, Fucus Vesiculosus, Hordeum Vulgare, Nasturtium Aquaticum, Raphanus Sativus, Triticum Aestivum, Iodium, Ubidecarenonum, Glandula Suprarenalis Suis, Hepar Suis, Manganese Gluconate, Oryza Sativa, Thyroidinum (Suis), Calcarea Carbonica, Natrum Muriaticum, Pulsatilla (Pratensis), Rhus Tox, Cortisone Aceticum).
What is the active ingredient?: Alfalfa, Avena sativa flowering top, Fucus vesiculosus, Hordeum vulgare top, Nasturtium officinale, Daikon, Triticum aestivum whole, Iodine, Ubidecarenone, Sus scrofa adrenal gland, Pork liver, Manganese gluconate, Brown rice, Thyroid, Oyster shell calcium carbonate, Crude, Sodium chloride, Pulsatilla pratensis whole, Toxicodendron pubescens leaf, Cortisone acetate.
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 Universaltox?: 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.