Home NDC 62795-9494-2 Zeel
Product NDC 62795-9494
Requested package NDC 62795-9494-2
11-digit product format 627959494
Labeler code 62795
Product ID 62795-9494_704bf227-bba9-427d-8d93-7cbf2497dcb5
Type HUMAN OTC DRUG
Nonproprietary name ALPHA LIPOIC ACID, ARNICA MONTANAROOT,SUS SCROFA CARTILAGE,COENZYME A, SOLANUM DULCAMARA TOP, SUS SCROFA EMBRYO,SUS SCROFA UMBILICAL CORD,NADIDE,SODIUM DIETHYL OXALACETATE, SUS SCROFA PLACENTA,TOXICODENDRON PUBESCENS LEAF,SANGUINARIA CANADENSIS ROOT,SILICON DIOXIDE,SULFUR,COMFREY ROOT
Dosage form TABLET
Route ORAL
Labeler MediNatura Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2022-01-12
Marketing end 0000-00-00
Substance ALPHA LIPOIC ACID; ARNICA MONTANA ROOT; SUS SCROFA CARTILAGE; COENZYME A; SOLANUM DULCAMARA TOP; SUS SCROFA EMBRYO; SUS SCROFA UMBILICAL CORD; NADIDE; SODIUM DIETHYL OXALACETATE; SUS SCROFA PLACENTA; TOXICODENDRON PUBESCENS LEAF; SANGUINARIA CANADENSIS ROOT; SILICON DIOXIDE; SULFUR; COMFREY 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; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC exclude flag No
Listing certified through 2023-12-31
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 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 62795-9494-2 Zeel 100 in 1 BOTTLE TABLET 100 2 62795-9494-2 Zeel 1 in 1 CARTON TABLET 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62795-9494 ZEEL (ALPHA LIPOIC ACID, ARNICA MONTANAROOT,SUS SCROFA CARTILAGE,COENZYME A, SOLANUM DULCAMARA TOP, SUS SCROFA EMBRYO,SUS SCROFA UMBILICAL CORD,NADIDE,SODIUM DIETHYL OXALACETATE, SUS SCROFA PLACENTA,TOXICODENDRON PUBESCENS LEAF,SANGUINARIA CANADENSIS ROOT,SILICON DIOXIDE,SULFUR,COMFREY ROOT) TABLET [MEDINATURA INC] 2 Legacy NDC, 2 package rows 20230929_7d22f888-88fa-4ebc-9c29-edf1e3514f4d.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 62795-9494-2 62795949402 1 BOTTLE in 1 CARTON (62795-9494-2) > 100 TABLET in 1 BOTTLE 1 bottle 2022-01-12 0000-00-00 No No Current