Home NDC 62795-1040 T-Relief Pro Spasm
Product NDC 62795-1040
11-digit product format 627951040
Labeler code 62795
Product ID 62795-1040_f166307e-e042-45bd-a6ae-7451092b34b5
Type HUMAN OTC DRUG
Nonproprietary name ACONITUM NAPELLUS,AMANITA MUSCARIA FRUITING BODY, AMMONIUM BROMIDE, ATROPINE SULFATE, ATROPA BELLADONNA, MATRICARIA RECUTITA, CITRULLUS COLOCYNTHIS FRUIT PULP,MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, PASSIFLORA INCARNATA FLOWERING TOP, and VERATRUM ALBUM ROOT
Dosage form TABLET
Route ORAL
Labeler MediNatura Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2017-11-16
Marketing end 2025-04-30
Substance ACONITUM NAPELLUS; AMANITA MUSCARIA FRUITING BODY; AMMONIUM BROMIDE; ATROPINE SULFATE; ATROPA BELLADONNA; MATRICARIA RECUTITA; CITRULLUS COLOCYNTHIS FRUIT PULP; CUPRIC SULFATE; GELSEMIUM SEMPERVIRENS ROOT; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PASSIFLORA INCARNATA FLOWERING TOP; VERATRUM ALBUM ROOT
Active strength 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
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 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 62795-1040-2 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 62795-1040-2 f5e01cc5f278…a2eaf40c39c3…
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 62795-1040-2 62795104002 90 TABLET in 1 BOTTLE (62795-1040-2) 90 tablet 2017-11-16 0000-00-00 No No Current