T-Relief Extra Strength Cream NDC 62795-7007

NDC codes

FDA NDC Directory

Product NDC (as listed)62795-7007Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62795-7007Add 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
62795-7007-4	62795700704	85 g in 1 TUBE (62795-7007-4)Marketed from Sep 27, 2023
62795-7007-5	62795700705	227 g in 1 JAR (62795-7007-5)Marketed from Sep 27, 2023
62795-7007-6	62795700706	1 JAR in 1 CARTON (62795-7007-6) / 227 g in 1 JARMarketed from Jul 16, 2020
62795-7007-7	62795700707	1 TUBE in 1 CARTON (62795-7007-7) / 85 g in 1 TUBEMarketed from Oct 19, 2017

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 Cream
Generic name (nonproprietary): arnica montana, calendula officinalis flowering top, echinacea unspecified, aconitum napellus, achillea millefolium, hamamelis virginiana root bark stem bark, matricaria chamomilla, atropa belladonna, bellis perennis, ruta graveolens flowering top, baptisia tinctoria root, comfrey root and hypericum perforatum
Active ingredients: Arnica montana — 1 [hp_X]/gCalendula officinalis flowering top — 1 [hp_X]/gEchinacea, Unspecified — 1 [hp_X]/gAconitum napellus — 1 [hp_X]/gAchillea millefolium — 2 [hp_X]/gHamamelis virginiana root bark/stem bark — 2 [hp_X]/gMatricaria chamomilla — 2 [hp_X]/gAtropa belladonna — 2 [hp_X]/gBellis perennis — 2 [hp_X]/gRuta graveolens flowering top — 4 [hp_X]/gBaptisia tinctoria root — 4 [hp_X]/gComfrey root — 4 [hp_X]/gHypericum perforatum — 6 [hp_X]/g
Dosage form: Cream
Route: Topical
Labeler: MediNatura Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 19, 2017
Listing expires: Dec 31, 2026
Identifiers: Product ID 62795-7007_677f014e-daf5-40b4-8b5f-fbcb7db0f0aeSPL ID 677f014e-daf5-40b4-8b5f-fbcb7db0f0aeSPL set ID 12f6cf2f-a924-42b1-9ca0-c360c7a59244UNII O80TY208ZW, 18E7415PXQ, 4N9P6CC1DX, U0NQ8555JD, 2FXJ6SW4PK, T7S323PKJS, G0R4UBI2ZZ, WQZ3G9PF0H, 2HU33I03UY, N94C2U587S, 5EF0HWI5WU, M9VVZ08EKQ, XK4IUX8MNB

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

N462795700704 followed by a unit qualifier and the quantity

Package 62795-7007-04. 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 27, 2023.

Indications (excerpt from the label)

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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)