Celeragesic NDC 43742-2364

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-2364Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-2364Add 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
43742-2364-1	43742236401	30 mL in 1 BOTTLE, DROPPER (43742-2364-1)Marketed from Feb 18, 2026

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): Celeragesic
Generic name (nonproprietary): aconitum napellus, arnica montana, bellis perennis, bryonia (alba), calendula officinalis, chamomilla, echinacea (angustifolia), echinacea purpurea, funiculus umbilicalis suis, glandula suprarenalis suis, hamamelis virginiana, hepar sulphuris calcareum, hypericum perforatum, ledum palustre, millefolium, nadidum, pantothenic acid, rhus tox, sarcolacticum acidum, symphytum officinale
Active ingredients: Aconitum napellus whole — 12 [hp_X]/mLArnica montana whole — 4 [hp_X]/mLBellis perennis whole — 2 [hp_X]/mLBryonia alba root — 8 [hp_X]/mLCalendula officinalis flowering top — 1 [hp_X]/mLMatricaria chamomilla whole — 3 [hp_X]/mLEchinacea angustifolia whole — 1 [hp_X]/mLEchinacea purpurea whole — 2 [hp_X]/mLSus scrofa umbilical cord — 12 [hp_X]/mLSus scrofa adrenal gland — 12 [hp_X]/mLHamamelis virginiana root bark/stem bark — 1 [hp_X]/mLCalcium sulfide — 12 [hp_X]/mLHypericum perforatum whole — 3 [hp_X]/mLRhododendron tomentosum leafy twig — 4 [hp_X]/mLAchillea millefolium whole — 3 [hp_X]/mLNadide — 8 [hp_X]/mLPantothenic acid — 8 [hp_X]/mLToxicodendron pubescens leaf — 8 [hp_X]/mLLactic acid, L- — 8 [hp_X]/mLComfrey root — 8 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 18, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 43742-2364_f1cd371c-cbe8-41d7-8ab6-27253c669d79SPL ID f1cd371c-cbe8-41d7-8ab6-27253c669d79SPL set ID 18e573b8-dd8d-432a-90c3-84b8929a4039UNII U0NQ8555JD, O80TY208ZW, 2HU33I03UY, T7J046YI2B, 18E7415PXQ, G0R4UBI2ZZ, VB06AV5US8, QI7G114Y98, 118OYG6W3H, 398IYQ16YV, T7S323PKJS, 1MBW07J51Q, XK4IUX8MNB, 877L01IZ0P, 2FXJ6SW4PK, 0U46U6E8UK, 19F5HK2737, 6IO182RP7A, F9S9FFU82N, M9VVZ08EKQUPC 0810151880945

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

N443742236401 followed by a unit qualifier and the quantity

Package 43742-2364-01. 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 Feb 18, 2026.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • muscular pain • joint pain • bruising • sports injury 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)