T-Relief Extra Strength NDC 62795-2010

NDC codes

FDA NDC Directory

Product NDC (as listed)62795-2010Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62795-2010Add 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
62795-2010-4	62795201004	1 BOTTLE in 1 CARTON (62795-2010-4) / 50 mL in 1 BOTTLEMarketed from Nov 5, 2019

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): calendula officinalis flowering top, matricaria recutita, hamamelis virginiana root bark/stem bark, achillea millefolium, ruta graveolens flowering top, comfrey root, aconitum napellus, echinacea, unspecified, baptisia tinctoria root, atropa belladonna, arnica montana, bellis perennis and hypericum perforatum
Active ingredients: Calendula officinalis flowering top — 2 [hp_X]/50mLMatricaria recutita — 2 [hp_X]/50mLHamamelis virginiana root bark/stem bark — 3 [hp_X]/50mLAchillea millefolium — 2 [hp_X]/50mLRuta graveolens flowering top — 3 [hp_X]/50mLComfrey root — 8 [hp_X]/50mLAconitum napellus — 3 [hp_X]/50mLEchinacea, Unspecified — 2 [hp_X]/50mLBaptisia tinctoria root — 2 [hp_X]/50mLAtropa belladonna — 3 [hp_X]/50mLArnica montana — 3 [hp_X]/50mLBellis perennis — 2 [hp_X]/50mLHypericum perforatum — 3 [hp_X]/50mL
Dosage form: Solution/ drops
Route: Oral
Labeler: MediNatura Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 5, 2019
Listing expires: Dec 31, 2026
Identifiers: Product ID 62795-2010_b7adba46-235d-4d94-9184-fe03eaf54102SPL ID b7adba46-235d-4d94-9184-fe03eaf54102SPL set ID 01804104-32c2-4011-a2e4-0f4e74bd974dUNII 18E7415PXQ, G0R4UBI2ZZ, T7S323PKJS, 2FXJ6SW4PK, N94C2U587S, M9VVZ08EKQ, U0NQ8555JD, 4N9P6CC1DX, 5EF0HWI5WU, WQZ3G9PF0H, O80TY208ZW, 2HU33I03UY, 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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N462795201004 followed by a unit qualifier and the quantity

Package 62795-2010-04. 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 28, 2023.

Indications (excerpt from the label)

USES Uses For the temporary relief of minor: Muscular 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)