Home NDC 62795-7008-7 T-Relief Pro Cream
Product NDC 62795-7008
Requested package NDC 62795-7008-7
11-digit product format 627957008
Labeler code 62795
Product ID 62795-7008_35a4ccd6-a31c-459c-b05b-fa4dc5c976cc
Type HUMAN OTC DRUG
Nonproprietary name 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
Dosage form CREAM
Route TOPICAL
Labeler Medinatura New Mexico, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2018-06-11
Marketing end 2022-07-31
Substance 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; HYPERICUM PERFORATUM
Active strength 1 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
NDC exclude flag No
Listing certified through 0000-00-00
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 62795-7008-7 62795700807 1 TUBE in 1 CARTON (62795-7008-7) > 85 g in 1 TUBE 1 tube 2018-06-11 2022-07-31 No No Current