T-Relief Extra Strength NDC 62795-1041

NDC codes

FDA NDC Directory

Product NDC (as listed)62795-1041Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62795-1041Add 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
62795-1041-3	62795104103	4 TABLET, CHEWABLE in 1 POUCH (62795-1041-3)Marketed from May 1, 2019
62795-1041-4	62795104104	1 BOTTLE in 1 CARTON (62795-1041-4) / 100 TABLET, CHEWABLE in 1 BOTTLEMarketed from Apr 7, 2021
62795-1041-5	62795104105	250 TABLET, CHEWABLE in 1 BOTTLE (62795-1041-5)Marketed from Apr 5, 2022
62795-1041-6	62795104106	100 TABLET, CHEWABLE in 1 BOTTLE (62795-1041-6)Marketed from Nov 22, 2022
62795-1041-7	62795104107	60 TABLET, CHEWABLE in 1 BOTTLE (62795-1041-7)Marketed from Sep 18, 2023

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): T-Relief Extra Strength
Generic name (nonproprietary): arnica montana, calendula officinalis flowering, hamamelis virginiana root bark/stem, baptisia tinctoria root, bellis perennis, echinacea, unspecified, aconitum napellus, matricaria chamomilla, achillea millefolium, atropa belladonna, hypericum perforatum, ruta graveolens flowering top and comfrey root
Active ingredients: Arnica montana — 3 [hp_X]/1Calendula officinalis flowering top — 2 [hp_X]/1Hamamelis virginiana root bark/stem bark — 2 [hp_X]/1Baptisia tinctoria root — 2 [hp_X]/1Bellis perennis — 2 [hp_X]/1Echinacea, Unspecified — 2 [hp_X]/1Aconitum napellus — 3 [hp_X]/1Matricaria chamomilla — 2 [hp_X]/1Achillea millefolium — 2 [hp_X]/1Atropa belladonna — 3 [hp_X]/1Hypericum perforatum — 3 [hp_X]/1Ruta graveolens flowering top — 3 [hp_X]/1Comfrey root — 6 [hp_X]/1
Dosage form: Tablet, Chewable
Route: Oral
Labeler: MediNatura Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 1, 2018
Listing expires: Dec 31, 2026
Identifiers: Product ID 62795-1041_ef7a3bff-c818-4f4c-bd31-98e1b7be7eeeSPL ID ef7a3bff-c818-4f4c-bd31-98e1b7be7eeeSPL set ID 97959b87-690d-45c1-9319-c17cdfa85020UNII O80TY208ZW, 18E7415PXQ, T7S323PKJS, 5EF0HWI5WU, 2HU33I03UY, 4N9P6CC1DX, U0NQ8555JD, G0R4UBI2ZZ, 2FXJ6SW4PK, WQZ3G9PF0H, XK4IUX8MNB, N94C2U587S, M9VVZ08EKQ

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

N462795104103 followed by a unit qualifier and the quantity

Package 62795-1041-03. 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 Sep 18, 2023.

Indications (excerpt from the label)

USES For the temporary relief of minor: • Joint Pain • Back Pain • Muscular Pain • Arthritis Pain

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)