Celeragesic NDC 43742-2248

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-2248Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-2248Add 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
43742-2248-1	43742224801	30 mL in 1 BOTTLE, DROPPER (43742-2248-1)Marketed from Mar 13, 2025

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 — 16 [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: Mar 13, 2025
Marketing end: Jan 7, 2030
Identifiers: Product ID 43742-2248_4fd9d1e8-7dfd-455a-938b-1472582cdde0SPL ID 4fd9d1e8-7dfd-455a-938b-1472582cdde0SPL set ID 2c328b15-7f00-479c-908b-88c1e5a52398UNII 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

N443742224801 followed by a unit qualifier and the quantity

Package 43742-2248-01. 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 6, 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)