What is NDC 43742-1493?

43742-1493 is the product NDC for Bio Cytotox Phase, Podophyllum 5 [hp_X]/mL + 27 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 Cytotox Phase (Podophyllum Peltatum, Ascorbicum Acidum, Galium Aparine, Hydrastis Canadensis, Nicotinamidum, Pyridoxinum Hydrochloricum, Riboflavinum, Sarcolacticum Acidum, Thiaminum Hydrochloricum, alpha-Lipoicum Acidum, Colchicum Autumnale, Conium Maculatum, Natrum Oxalaceticum, Sulphur, Vaccinium Myrtillus, Norepinephrine, Acetylsalicylicum Acidum, Adenosinum Triphosphoricum Dinatrum, Anthrachinonum, Histaminum Hydrochloricum, Magnesium Gluconicum Dihydricum, Nadidum, Naphthochinonum, Pantothenic Acid, Ubidecarenonum,).

What is the active ingredient?

Podophyllum, Ascorbic acid, Galium aparine, Goldenseal, Niacinamide, Pyridoxine hydrochloride, Riboflavin, Lactic acid, L-, Thiamine hydrochloride, Thioctic acid, Colchicum autumnale bulb, Conium maculatum flowering top, Sodium diethyl oxalacetate, Sulfur, Bilberry, Norepinephrine bitartrate, Aspirin, Adenosine triphosphate disodium, Anthraquinone, Histamine dihydrochloride, Magnesium gluconate, Nadide, Naphthoquine, Ubidecarenone, Pantothenic acid, Manganese phosphate, Dibasic, Hydroquinone, Salmonella enterica subsp. Enterica serovar enteritidis.

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 Cytotox 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 Cytotox Phase NDC 43742-1493 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1493Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1493Add 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
43742-1493-1	4374214930143742149301	30 mL in 1 BOTTLE, DROPPER (43742-1493-1)Marketed from Jul 9, 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 Cytotox Phase
Generic name (nonproprietary): podophyllum peltatum, ascorbicum acidum, galium aparine, hydrastis canadensis, nicotinamidum, pyridoxinum hydrochloricum, riboflavinum, sarcolacticum acidum, thiaminum hydrochloricum, alpha-lipoicum acidum, colchicum autumnale, conium maculatum, natrum oxalaceticum, sulphur, vaccinium myrtillus, norepinephrine, acetylsalicylicum acidum, adenosinum triphosphoricum dinatrum, anthrachinonum, histaminum hydrochloricum, magnesium gluconicum dihydricum, nadidum, naphthochinonum, pantothenic acid, ubidecarenonum,
Active ingredients: Podophyllum — 5 [hp_X]/mLAscorbic acid — 6 [hp_X]/mLGalium aparine — 6 [hp_X]/mLGoldenseal — 6 [hp_X]/mLNiacinamide — 6 [hp_X]/mLPyridoxine hydrochloride — 6 [hp_X]/mLRiboflavin — 6 [hp_X]/mLLactic acid, L- — 6 [hp_X]/mLThiamine hydrochloride — 6 [hp_X]/mLThioctic acid — 8 [hp_X]/mLColchicum autumnale bulb — 8 [hp_X]/mLConium maculatum flowering top — 8 [hp_X]/mLSodium diethyl oxalacetate — 8 [hp_X]/mLSulfur — 8 [hp_X]/mLBilberry — 8 [hp_X]/mLNorepinephrine bitartrate — 10 [hp_X]/mLAspirin — 10 [hp_X]/mLAdenosine triphosphate disodium — 10 [hp_X]/mLAnthraquinone — 10 [hp_X]/mLHistamine dihydrochloride — 10 [hp_X]/mLMagnesium gluconate — 10 [hp_X]/mLNadide — 10 [hp_X]/mLNaphthoquine — 10 [hp_X]/mLUbidecarenone — 10 [hp_X]/mLPantothenic acid — 10 [hp_X]/mLManganese phosphate, Dibasic — 15 [hp_X]/mLHydroquinone — 3 [hp_C]/mLSalmonella enterica subsp. Enterica serovar enteritidis — 30 [hp_C]/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: Jul 9, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Analogs/Derivatives (Chemical/Ingredient)Non-Steroidal (Chemical structure)Ascorbic Acid (Chemical structure)Catecholamines (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Decreased Platelet Aggregation (Physiologic effect)Decreased Prostaglandin Production (Physiologic effect)Depigmenting Activity (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Magnetic Resonance Contrast Activity (Mechanism)Melanin Synthesis Inhibitors (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)Vitamin B 6 (Chemical/Ingredient)
Identifiers: Product ID 43742-1493_a656929e-6959-45b3-a335-1e8bcb88718dSPL ID a656929e-6959-45b3-a335-1e8bcb88718dSPL set ID ca632470-6cbc-4994-a7f0-95b6ad9aa44fUNII 2S713A4VP3, PQ6CK8PD0R, Z4B6561488, ZW3Z11D0JV, 25X51I8RD4, 68Y4CF58BV, TLM2976OFR, F9S9FFU82N, M572600E5P, 73Y7P0K73Y, 993QHL78E6, Q28R5GF371, 6CA025Y4FG, 70FD1KFU70, 9P2U39H18W, IFY5PE3ZRW, R16CO5Y76E, 5L51B4DR1G, 030MS0JBDO, 3POA0Q644U, T42NAD2KHC, 0U46U6E8UK, TRY8UD4E2H, EJ27X76M46, 19F5HK2737, VZ3U1H7Q5B, XV74C1N1AE, Y3V16D4PV4UPC 0810151881737
Pharmacologic class: Calculi Dissolution Agent; Catecholamine; Melanin Synthesis Inhibitor; Nonsteroidal Anti-inflammatory Drug; Osmotic Laxative; Paramagnetic Contrast Agent; Platelet Aggregation Inhibitor; Vitamin B6 Analog; Vitamin C

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

N443742149301 followed by a unit qualifier and the quantity

Package 43742-1493-01. 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 14, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • metabolism support • fatigue • weakened constitution 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 43742-1493

What is NDC 43742-1493?: 43742-1493 is the product NDC for Bio Cytotox Phase, Podophyllum 5 [hp_X]/mL + 27 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 Cytotox Phase (Podophyllum Peltatum, Ascorbicum Acidum, Galium Aparine, Hydrastis Canadensis, Nicotinamidum, Pyridoxinum Hydrochloricum, Riboflavinum, Sarcolacticum Acidum, Thiaminum Hydrochloricum, alpha-Lipoicum Acidum, Colchicum Autumnale, Conium Maculatum, Natrum Oxalaceticum, Sulphur, Vaccinium Myrtillus, Norepinephrine, Acetylsalicylicum Acidum, Adenosinum Triphosphoricum Dinatrum, Anthrachinonum, Histaminum Hydrochloricum, Magnesium Gluconicum Dihydricum, Nadidum, Naphthochinonum, Pantothenic Acid, Ubidecarenonum,).
What is the active ingredient?: Podophyllum, Ascorbic acid, Galium aparine, Goldenseal, Niacinamide, Pyridoxine hydrochloride, Riboflavin, Lactic acid, L-, Thiamine hydrochloride, Thioctic acid, Colchicum autumnale bulb, Conium maculatum flowering top, Sodium diethyl oxalacetate, Sulfur, Bilberry, Norepinephrine bitartrate, Aspirin, Adenosine triphosphate disodium, Anthraquinone, Histamine dihydrochloride, Magnesium gluconate, Nadide, Naphthoquine, Ubidecarenone, Pantothenic acid, Manganese phosphate, Dibasic, Hydroquinone, Salmonella enterica subsp. Enterica serovar enteritidis.
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 Cytotox 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.