Oral Health NDC 43742-1592

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1592Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1592Add 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
43742-1592-1	43742159201	30 mL in 1 BOTTLE, DROPPER (43742-1592-1)Marketed from Feb 19, 2020

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): borax, 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
Active ingredients: Sodium borate — 6 [hp_X]/mLBryonia alba root — 6 [hp_X]/mLEchinacea purpurea whole — 6 [hp_X]/mLJuglans cinerea branch bark/root bark — 6 [hp_X]/mLPotassium chloride — 6 [hp_X]/mLMagnesium chloride — 6 [hp_X]/mLHydrochloric acid — 6 [hp_X]/mLSus scrofa intervertebral disc — 8 [hp_X]/mLSus scrofa oral mucosa — 8 [hp_X]/mLAntimony trisulfide — 12 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLBismuth subnitrate — 12 [hp_X]/mLMatricaria chamomilla whole — 12 [hp_X]/mLCinchona officinalis bark — 12 [hp_X]/mLNutmeg — 12 [hp_X]/mLSambucus nigra flowering top — 12 [hp_X]/mLSepia officinalis juice — 12 [hp_X]/mLMercurius solubilis — 12 [hp_X]/mLTribasic calcium phosphate — 12 [hp_X]/mLStrychnos ignatii seed — 12 [hp_X]/mLOxygen — 16 [hp_X]/mLCandida albicans — 16 [hp_X]/mLStaphylococcus aureus — 12 [hp_C]/mLStreptococcus mutans — 12 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 19, 2020
Marketing end: Sep 19, 2028
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 43742-1592_6b4e2e0f-87a7-4816-8d63-6423ca6794c4SPL ID 6b4e2e0f-87a7-4816-8d63-6423ca6794c4SPL set ID 81ffb30f-5255-4e16-ba9d-b0de909aa557UNII 91MBZ8H3QO, T7J046YI2B, QI7G114Y98, 48FZ1BHO18, 660YQ98I10, 02F3473H9O, QTT17582CB, OJ17O2WTSM, DUP6W562BM, F79059A38U, S7V92P67HO, H19J064BA5, G0R4UBI2ZZ, S003A158SB, AEE24M3MQ9, CT03BSA18U, QDL83WN8C2, 324Y4038G2, 91D9GV0Z28, 1NM3M2487K, S88TT14065, 4D7G21HDBC, O478WX4004, 5C7J33MJJ1
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

N443742159201 followed by a unit qualifier and the quantity

Package 43742-1592-01. 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 5, 2024.

Indications (excerpt from the label)

HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms related to oral health, such as cavitation, delayed dentition, dry mouth, painful eating, eruptions on tongue and inner cheeks and tooth sensitivity.** **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)