Celeragesic NDC 43742-2243

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-2243Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-2243Add 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
43742-2243-1	43742224301	57 g in 1 TUBE (43742-2243-1)Marketed from Jan 14, 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): echinacea (angustifolia), calendula officinalis, hamamelis virginiana, echinacea purpurea, bellis perennis, chamomilla, hypericum perforatum, millefolium, ledum palustre, arnica montana, bryonia (alba), nadidum, pantothenic acid, sarcolacticum acidum, symphytum officinale, rhus tox, aconitum napellus, funiculus umbilicalis suis, glandula suprarenalis suis, hepar sulphuris calcareum
Active ingredients: Echinacea angustifolia whole — 1 [hp_X]/gCalendula officinalis flowering top — 1 [hp_X]/gHamamelis virginiana root bark/stem bark — 1 [hp_X]/gEchinacea purpurea whole — 2 [hp_X]/gBellis perennis whole — 2 [hp_X]/gMatricaria chamomilla whole — 3 [hp_X]/gHypericum perforatum whole — 3 [hp_X]/gAchillea millefolium whole — 3 [hp_X]/gRhododendron tomentosum leafy twig — 4 [hp_X]/gArnica montana whole — 4 [hp_X]/gBryonia alba root — 8 [hp_X]/gNadide — 8 [hp_X]/gPantothenic acid — 8 [hp_X]/gLactic acid, L- — 8 [hp_X]/gComfrey root — 8 [hp_X]/gToxicodendron pubescens leaf — 8 [hp_X]/gAconitum napellus whole — 12 [hp_X]/gSus scrofa umbilical cord — 12 [hp_X]/gSus scrofa adrenal gland — 12 [hp_X]/gCalcium sulfide — 30 [hp_X]/g
Dosage form: Gel
Route: Topical
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 14, 2025
Listing expires: Dec 31, 2026
Identifiers: Product ID 43742-2243_9c99e905-07cd-41c8-887d-d8e0ae04c751SPL ID 9c99e905-07cd-41c8-887d-d8e0ae04c751SPL set ID 1a3edb9d-e571-4275-b56e-d2489da11e76UNII VB06AV5US8, 18E7415PXQ, T7S323PKJS, QI7G114Y98, 2HU33I03UY, G0R4UBI2ZZ, XK4IUX8MNB, 2FXJ6SW4PK, 877L01IZ0P, O80TY208ZW, T7J046YI2B, 0U46U6E8UK, 19F5HK2737, F9S9FFU82N, M9VVZ08EKQ, 6IO182RP7A, U0NQ8555JD, 118OYG6W3H, 398IYQ16YV, 1MBW07J51QUPC 0810151883410

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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N443742224301 followed by a unit qualifier and the quantity

Package 43742-2243-01. 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 Jan 14, 2025.

Indications (excerpt from the label)

INDICATIONS: For the temporary relief of muscular pain, joint pain, sports injuries and bruising.** **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)