Celeragesic NDC 43742-1267

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1267Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1267Add 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
43742-1267-1	43742126701	30 mL in 1 BOTTLE, DROPPER (43742-1267-1)Marketed from Sep 4, 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]/mLCalendula officinalis flowering top — 1 [hp_X]/mLHamamelis virginiana root bark/stem bark — 1 [hp_X]/mLEchinacea purpurea whole — 2 [hp_X]/mLBellis perennis whole — 2 [hp_X]/mLMatricaria chamomilla whole — 3 [hp_X]/mLHypericum perforatum whole — 3 [hp_X]/mLAchillea millefolium whole — 3 [hp_X]/mLRhododendron tomentosum leafy twig — 4 [hp_X]/mLArnica montana whole — 4 [hp_X]/mLBryonia alba root — 8 [hp_X]/mLCalcium sulfide — 8 [hp_X]/mLNadide — 8 [hp_X]/mLPantothenic acid — 8 [hp_X]/mLLactic acid, L- — 8 [hp_X]/mLComfrey root — 8 [hp_X]/mLToxicodendron pubescens leaf — 8 [hp_X]/mLAconitum napellus whole — 12 [hp_X]/mLSus scrofa umbilical cord — 12 [hp_X]/mLSus scrofa adrenal gland — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 4, 2018
Marketing end: May 22, 2029
Identifiers: Product ID 43742-1267_8b73b96a-9f1a-4c60-8ddc-51db1fa2c028SPL ID 8b73b96a-9f1a-4c60-8ddc-51db1fa2c028SPL set ID d3d8a7f4-169c-4780-852d-c96a4772e7e3UNII VB06AV5US8, 18E7415PXQ, T7S323PKJS, QI7G114Y98, 2HU33I03UY, G0R4UBI2ZZ, XK4IUX8MNB, 2FXJ6SW4PK, 877L01IZ0P, O80TY208ZW, T7J046YI2B, 1MBW07J51Q, 0U46U6E8UK, 19F5HK2737, F9S9FFU82N, M9VVZ08EKQ, 6IO182RP7A, U0NQ8555JD, 118OYG6W3H, 398IYQ16YVUPC 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

N443742126701 followed by a unit qualifier and the quantity

Package 43742-1267-01. 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)

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)