What is NDC 43742-2122?

43742-2122 is the product NDC for Oral Health, Antimony trisulfide 12 [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?

Oral Health (Antimonium Crudum, Arsenicum Album, Bismuthum Subnitricum, Borax, Bryonia (Alba), Calcarea Phosphorica, Candida Albicans, Chamomilla, Cinchona Officinalis, Discus Intervertebralis Suis, Streptococcus Dysgalactiae DNA, Streptococcus Mutans DNA, Streptococcus Pneumoniae DNA, Echinacea Purpurea, Ignatia Amara, Juglans Cinerea, Kali Muriaticum, Magnesia Muriatica, Mercurius Solubilis, Muriaticum Acidum, Nux Moschata, Oral Mucosa (Suis), Oxygenium, Sambucus Nigra, Sepia, Staphylococcus Aureus,).

What is the active ingredient?

Antimony trisulfide, Arsenic trioxide, Bismuth subnitrate, Sodium borate, Bryonia alba root, Tribasic calcium phosphate, Candida albicans, Matricaria chamomilla whole, Cinchona officinalis bark, Sus scrofa intervertebral disc, Herring sperm DNA, Echinacea purpurea whole, Strychnos ignatii seed, Juglans cinerea branch bark/root bark, Potassium chloride, Magnesium chloride, Mercurius solubilis, Hydrochloric acid, Nutmeg, Sus scrofa oral mucosa, Oxygen, Sambucus nigra flowering top, Sepia officinalis juice, Staphylococcus aureus, Streptococcus mutans.

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 Oral Health?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Oral Health NDC 43742-2122 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-2122Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-2122Add 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
43742-2122-1	4374221220143742212201	30 mL in 1 BOTTLE, DROPPER (43742-2122-1)Marketed from Apr 1, 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): Oral Health
Generic name (nonproprietary): antimonium crudum, arsenicum album, bismuthum subnitricum, borax, bryonia (alba), calcarea phosphorica, candida albicans, chamomilla, cinchona officinalis, discus intervertebralis suis, streptococcus dysgalactiae dna, streptococcus mutans dna, streptococcus pneumoniae dna, echinacea purpurea, ignatia amara, juglans cinerea, kali muriaticum, magnesia muriatica, mercurius solubilis, muriaticum acidum, nux moschata, oral mucosa (suis), oxygenium, sambucus nigra, sepia, staphylococcus aureus,
Active ingredients: Antimony trisulfide — 12 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLBismuth subnitrate — 12 [hp_X]/mLSodium borate — 6 [hp_X]/mLBryonia alba root — 6 [hp_X]/mLTribasic calcium phosphate — 12 [hp_X]/mLCandida albicans — 16 [hp_X]/mLMatricaria chamomilla whole — 12 [hp_X]/mLCinchona officinalis bark — 12 [hp_X]/mLSus scrofa intervertebral disc — 8 [hp_X]/mLHerring sperm DNA — 12 [hp_C]/mLEchinacea purpurea whole — 6 [hp_X]/mLStrychnos ignatii seed — 12 [hp_X]/mLJuglans cinerea branch bark/root bark — 6 [hp_X]/mLPotassium chloride — 6 [hp_X]/mLMagnesium chloride — 6 [hp_X]/mLMercurius solubilis — 12 [hp_X]/mLHydrochloric acid — 6 [hp_X]/mLNutmeg — 12 [hp_X]/mLSus scrofa oral mucosa — 8 [hp_X]/mLOxygen — 16 [hp_X]/mLSambucus nigra flowering top — 12 [hp_X]/mLSepia officinalis juice — 12 [hp_X]/mLStaphylococcus aureus — 12 [hp_C]/mLStreptococcus mutans — 12 [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: Apr 1, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Bismuth (Chemical structure)Calcium (Chemical structure)Divalent (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Fungal Proteins (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (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)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Plant Proteins (Chemical structure)Potassium Compounds (Chemical structure)Seed Storage Proteins (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 43742-2122_a1f631c4-9d16-4c0e-a2dd-0edd6e5db87aSPL ID a1f631c4-9d16-4c0e-a2dd-0edd6e5db87aSPL set ID 6f66ff40-6e0e-4a35-963c-965c65df76ebUNII F79059A38U, S7V92P67HO, H19J064BA5, 91MBZ8H3QO, T7J046YI2B, 91D9GV0Z28, 4D7G21HDBC, G0R4UBI2ZZ, S003A158SB, OJ17O2WTSM, 51FI676N6F, QI7G114Y98, 1NM3M2487K, 48FZ1BHO18, 660YQ98I10, 02F3473H9O, 324Y4038G2, QTT17582CB, AEE24M3MQ9, DUP6W562BM, S88TT14065, CT03BSA18U, QDL83WN8C2, O478WX4004, 5C7J33MJJ1UPC 0810151883779
Pharmacologic class: Bismuth; Blood Coagulation Factor; Calculi Dissolution Agent; Non-Standardized Food Allergenic Extract; Non-Standardized Fungal Allergenic Extract; Non-Standardized Plant Allergenic Extract; Osmotic Laxative; Phosphate Binder; 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

N443742212201 followed by a unit qualifier and the quantity

Package 43742-2122-01. 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 Apr 1, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • mouth support • teeth sensitivity • dental issues • dental support • pain in ears • eruption on tongue • eruption on cheeks • dry mouth 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 43742-2122

What is NDC 43742-2122?: 43742-2122 is the product NDC for Oral Health, Antimony trisulfide 12 [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?: Oral Health (Antimonium Crudum, Arsenicum Album, Bismuthum Subnitricum, Borax, Bryonia (Alba), Calcarea Phosphorica, Candida Albicans, Chamomilla, Cinchona Officinalis, Discus Intervertebralis Suis, Streptococcus Dysgalactiae DNA, Streptococcus Mutans DNA, Streptococcus Pneumoniae DNA, Echinacea Purpurea, Ignatia Amara, Juglans Cinerea, Kali Muriaticum, Magnesia Muriatica, Mercurius Solubilis, Muriaticum Acidum, Nux Moschata, Oral Mucosa (Suis), Oxygenium, Sambucus Nigra, Sepia, Staphylococcus Aureus,).
What is the active ingredient?: Antimony trisulfide, Arsenic trioxide, Bismuth subnitrate, Sodium borate, Bryonia alba root, Tribasic calcium phosphate, Candida albicans, Matricaria chamomilla whole, Cinchona officinalis bark, Sus scrofa intervertebral disc, Herring sperm DNA, Echinacea purpurea whole, Strychnos ignatii seed, Juglans cinerea branch bark/root bark, Potassium chloride, Magnesium chloride, Mercurius solubilis, Hydrochloric acid, Nutmeg, Sus scrofa oral mucosa, Oxygen, Sambucus nigra flowering top, Sepia officinalis juice, Staphylococcus aureus, Streptococcus mutans.
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 Oral Health?: 1 other product NDC are listed under this name. See all Oral Health NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Oral Health NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Oral Healthborax, bryonia (alba), echinacea purpurea, juglans cinerea, kali muriaticum, magnesia muriatica, muriaticum acidum, discus intervertebralis suis, oral mucosa (suis), antimonium crudum, arsenicum album, bismuthum subnitricum, chamomilla, cinchona officinalis, nux moschata, sambucus nigra, sepia, mercurius solubilis, calcarea phosphorica, ignatia amara, oxygenium, candida albicans, staphylococcus aureus, streptococcus mutans	Sodium borate 6 [hp_X]/mL + 23 more ingredients	LiquidOral	Deseret Biologicals, Inc.	43742-1592	43742-1592-01