Celeragesic NDC 43742-1397

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1397Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1397Add 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
43742-1397-1	43742139701	57 g in 1 TUBE (43742-1397-1)Marketed from Oct 31, 2018

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), hepar sulphuris calcareum, nadidum, pantothenic acid, sarcolacticum acidum, symphytum officinale, rhus tox, aconitum napellus, funiculus umbilicalis suis, glandula suprarenalis suis
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]/gCalcium sulfide — 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]/g
Dosage form: Gel
Route: Topical
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 31, 2018
Marketing end: Mar 4, 2029
Identifiers: Product ID 43742-1397_6013ce10-fc4f-4409-8817-1db1a9e4d65eSPL ID 6013ce10-fc4f-4409-8817-1db1a9e4d65eSPL set ID aa8f0dd4-4a3e-49ab-85cf-e4a5f48cdbf5UNII VB06AV5US8, 18E7415PXQ, T7S323PKJS, QI7G114Y98, 2HU33I03UY, G0R4UBI2ZZ, XK4IUX8MNB, 2FXJ6SW4PK, 877L01IZ0P, O80TY208ZW, T7J046YI2B, 1MBW07J51Q, 0U46U6E8UK, 19F5HK2737, F9S9FFU82N, M9VVZ08EKQ, 6IO182RP7A, U0NQ8555JD, 118OYG6W3H, 398IYQ16YVUPC 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

N443742139701 followed by a unit qualifier and the quantity

Package 43742-1397-01. 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 Oct 22, 2024.

Indications (excerpt from the label)

HOMEOPATHIC 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)