Home NDC 62795-1023 BHI Cold
Product NDC 62795-1023
11-digit product format 627951023
Labeler code 62795
Product ID 62795-1023_0796514f-7864-45a2-8894-9bb66517de72
Type HUMAN OTC DRUG
Nonproprietary name PULSATILLA VULGARIS and SULFUR
Dosage form TABLET
Route ORAL
Labeler MediNatura Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2014-08-30
Marketing end 2025-02-28
Substance PULSATILLA VULGARIS; SULFUR
Active strength 6 [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 · 12 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 62795-1023-3 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 62795-1023-3 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 62795-1023-3 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 62795-1023-3 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 62795-1023-3 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 62795-1023-3 cdf11ea48f46…ba0047e9e063…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 62795-1023-2 62795102302 100 TABLET in 1 BOTTLE (62795-1023-2) 100 tablet 2014-08-30 0000-00-00 No No Current 62795-1023-3 62795102303 1 BOTTLE in 1 CARTON (62795-1023-3) > 100 TABLET in 1 BOTTLE 1 bottle 2014-08-30 2025-02-28 No No Current