What is NDC 43742-1257?

43742-1257 is the product NDC for Bio Glyoxal Phase, Arnica montana whole 4 [hp_X]/mL + 24 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Bio Glyoxal Phase (Arnica Montana, Baptisia Tinctoria, Echinacea (Angustifolia), Sanguinaria Canadensis, Eupatorium Perfoliatum, Euphorbium Officinarum, Dopamine Hydrochloride, Phytolacca Decandra, Aconitum Napellus, Argentum Nitricum, Arsenicum Album, Bryonia (Alba), Gelsemium Sempervirens, Mercurius Corrosivus, Phosphorus, Pulsatilla (Pratensis), Rhus Tox, Sulphur, Thuja Occidentalis, Cortisone Aceticum, Acetaldehyde, Formalinum, Hepar Sulphuris Calcareum, Lachesis Mutus, Zincum Metallicum).

What is the active ingredient?

Arnica montana whole, Baptisia tinctoria root, Echinacea angustifolia whole, Sanguinaria canadensis root, Eupatorium perfoliatum flowering top, Euphorbia resinifera resin, Dopamine hydrochloride, Phytolacca americana root, Aconitum napellus whole, Silver nitrate, Arsenic trioxide, Bryonia alba root, Gelsemium sempervirens root, Mercuric chloride, Phosphorus, Pulsatilla pratensis whole, Toxicodendron pubescens leaf, Sulfur, Thuja occidentalis leafy twig, Cortisone acetate, Acetaldehyde, Formaldehyde, Calcium sulfide, Lachesis muta venom, Zinc.

Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Bio Glyoxal Phase?

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.

Bio Glyoxal Phase NDC 43742-1257 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1257Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1257Add 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
43742-1257-1	4374212570143742125701	30 mL in 1 BOTTLE, DROPPER (43742-1257-1)Marketed from Jun 7, 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): Bio Glyoxal Phase
Generic name (nonproprietary): arnica montana, baptisia tinctoria, echinacea (angustifolia), sanguinaria canadensis, eupatorium perfoliatum, euphorbium officinarum, dopamine hydrochloride, phytolacca decandra, aconitum napellus, argentum nitricum, arsenicum album, bryonia (alba), gelsemium sempervirens, mercurius corrosivus, phosphorus, pulsatilla (pratensis), rhus tox, sulphur, thuja occidentalis, cortisone aceticum, acetaldehyde, formalinum, hepar sulphuris calcareum, lachesis mutus, zincum metallicum
Active ingredients: Arnica montana whole — 4 [hp_X]/mLBaptisia tinctoria root — 4 [hp_X]/mLEchinacea angustifolia whole — 5 [hp_X]/mLSanguinaria canadensis root — 5 [hp_X]/mLEupatorium perfoliatum flowering top — 6 [hp_X]/mLEuphorbia resinifera resin — 6 [hp_X]/mLDopamine hydrochloride — 6 [hp_X]/mLPhytolacca americana root — 7 [hp_X]/mLAconitum napellus whole — 8 [hp_X]/mLSilver nitrate — 8 [hp_X]/mLArsenic trioxide — 8 [hp_X]/mLBryonia alba root — 8 [hp_X]/mLGelsemium sempervirens root — 8 [hp_X]/mLMercuric chloride — 8 [hp_X]/mLPhosphorus — 8 [hp_X]/mLPulsatilla pratensis whole — 8 [hp_X]/mLToxicodendron pubescens leaf — 8 [hp_X]/mLSulfur — 8 [hp_X]/mLThuja occidentalis leafy twig — 8 [hp_X]/mLCortisone acetate — 8 [hp_X]/mLAcetaldehyde — 10 [hp_X]/mLFormaldehyde — 10 [hp_X]/mLCalcium sulfide — 10 [hp_X]/mLLachesis muta venom — 10 [hp_X]/mLZinc — 10 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.NDC labeler code 43742
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 7, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Catecholamines (Chemical structure)Cell-mediated Immunity (Physiologic effect)Corticosteroid Hormone Receptor Agonists (Mechanism)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 43742-1257_03d71963-e6ad-4b8d-9563-baff77787b37SPL ID 03d71963-e6ad-4b8d-9563-baff77787b37SPL set ID d43db203-7756-43a5-bd68-aa070d429f60UNII O80TY208ZW, 5EF0HWI5WU, VB06AV5US8, N9288CD508, 1W0775VX6E, 1TI1O9028K, 7L3E358N9L, 11E6VI8VEG, U0NQ8555JD, 95IT3W8JZE, S7V92P67HO, T7J046YI2B, 639KR60Q1Q, 53GH7MZT1R, 27YLU75U4W, 8E272251DI, 6IO182RP7A, 70FD1KFU70, 1NT28V9397, 883WKN7W8X, GO1N1ZPR3B, 1HG84L3525, 1MBW07J51Q, VSW71SS07I, J41CSQ7QDSUPC 0810151881676
Pharmacologic class: Catecholamine; Corticosteroid; Standardized Chemical Allergen

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

N443742125701 followed by a unit qualifier and the quantity

Package 43742-1257-01. 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 May 9, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • cold symptoms • flu symptoms • low energy These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43742-1257

What is NDC 43742-1257?: 43742-1257 is the product NDC for Bio Glyoxal Phase, Arnica montana whole 4 [hp_X]/mL + 24 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Bio Glyoxal Phase (Arnica Montana, Baptisia Tinctoria, Echinacea (Angustifolia), Sanguinaria Canadensis, Eupatorium Perfoliatum, Euphorbium Officinarum, Dopamine Hydrochloride, Phytolacca Decandra, Aconitum Napellus, Argentum Nitricum, Arsenicum Album, Bryonia (Alba), Gelsemium Sempervirens, Mercurius Corrosivus, Phosphorus, Pulsatilla (Pratensis), Rhus Tox, Sulphur, Thuja Occidentalis, Cortisone Aceticum, Acetaldehyde, Formalinum, Hepar Sulphuris Calcareum, Lachesis Mutus, Zincum Metallicum).
What is the active ingredient?: Arnica montana whole, Baptisia tinctoria root, Echinacea angustifolia whole, Sanguinaria canadensis root, Eupatorium perfoliatum flowering top, Euphorbia resinifera resin, Dopamine hydrochloride, Phytolacca americana root, Aconitum napellus whole, Silver nitrate, Arsenic trioxide, Bryonia alba root, Gelsemium sempervirens root, Mercuric chloride, Phosphorus, Pulsatilla pratensis whole, Toxicodendron pubescens leaf, Sulfur, Thuja occidentalis leafy twig, Cortisone acetate, Acetaldehyde, Formaldehyde, Calcium sulfide, Lachesis muta venom, Zinc.
Who is the labeler?: Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Bio Glyoxal Phase?: 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.