T-Relief NDC 62795-1034

NDC codes

FDA NDC Directory

Product NDC (as listed)62795-1034Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62795-1034Add 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
62795-1034-2	62795103402	1 BOTTLE in 1 CARTON (62795-1034-2) / 100 TABLET, CHEWABLE in 1 BOTTLEMarketed from Dec 1, 2015
62795-1034-4	62795103404	100 TABLET, CHEWABLE in 1 BOTTLE (62795-1034-4)Marketed from Nov 16, 2022

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
Generic name (nonproprietary): arnica montana whole, calendula officinalis flowering top, hamamelis virginiana root bark/stem bark,baptisia tinctoria root, bellis perennis whole, echinacea angustifolia whole,aconitum napellus whole,matricaria chamomilla whole,achillea millefolium whole,atropa belladonna,hypericum perforatum whole,ruta graveolens flowering top and comfrey root
Active ingredients: Aconitum napellus — 3 [hp_M]/1Matricaria recutita — 2 [hp_X]/1Hamamelis virginiana root bark/stem bark — 2 [hp_X]/1Hypericum perforatum — 3 [hp_X]/1Ruta graveolens flowering top — 4 [hp_X]/1Comfrey root — 8 [hp_X]/1Baptisia tinctoria root — 2 [hp_X]/1Atropa belladonna — 3 [hp_X]/1Bellis perennis — 2 [hp_X]/1Calendula officinalis flowering top — 2 [hp_X]/1Echinacea angustifolia — 2 [hp_X]/1Arnica montana — 3 [hp_X]/1Achillea millefolium whole — 2 [hp_X]/1
Dosage form: Tablet, Chewable
Route: Oral
Labeler: MediNatura Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 1, 2015
Listing expires: Dec 31, 2026
Identifiers: Product ID 62795-1034_192c1cc3-f146-41ef-a532-e0fc1252f9adSPL ID 192c1cc3-f146-41ef-a532-e0fc1252f9adSPL set ID 2bd442ca-0bbe-0bc3-e054-00144ff8d46cUNII U0NQ8555JD, G0R4UBI2ZZ, T7S323PKJS, XK4IUX8MNB, N94C2U587S, M9VVZ08EKQ, 5EF0HWI5WU, WQZ3G9PF0H, 2HU33I03UY, 18E7415PXQ, VB06AV5US8, O80TY208ZW, 2FXJ6SW4PK

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

N462795103402 followed by a unit qualifier and the quantity

Package 62795-1034-02. 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 Mar 21, 2023.

Indications (excerpt from the label)

Uses For the temporary relief of minor: Muscle Pain, joint pain, back pain, nerve pain and Arthritis pain

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)