Home NDC 62795-9004-2 BHI Uri-Control
Product NDC 62795-9004
Requested package NDC 62795-9004-2
11-digit product format 627959004
Labeler code 62795
Product ID 62795-9004_739f2f93-cb22-42f4-ab70-d61518723e1a
Type HUMAN OTC DRUG
Nonproprietary name APIS MELLIFERA, SILVER NITRATE, ATROPA BELLADONNA, LYTTA VESICATORIA, CAUSTICUM, EQUISETUM HYEMALE, PETROSELINUM CRISPUM, PULSATILLA VULGARIS, SMILAX REGELII ROOT, and TURPENTINE OIL
Dosage form TABLET
Route ORAL
Labeler MediNatura Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2022-02-21
Marketing end 0000-00-00
Substance APIS MELLIFERA; ATROPA BELLADONNA; CAUSTICUM; EQUISETUM HYEMALE; LYTTA VESICATORIA; PETROSELINUM CRISPUM; PULSATILLA VULGARIS; SILVER NITRATE; SMILAX ORNATA ROOT; TURPENTINE OIL
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
Pharmacologic classes Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]
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.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 62795-9004-2 BHI Uri-Control 1 in 1 CARTON TABLET 1 2 62795-9004-2 BHI Uri-Control 100 in 1 BOTTLE TABLET 100 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62795-9004 BHI URI-CONTROL (APIS MELLIFERA, SILVER NITRATE, ATROPA BELLADONNA, LYTTA VESICATORIA, CAUSTICUM, EQUISETUM HYEMALE, PETROSELINUM CRISPUM, PULSATILLA VULGARIS, SMILAX REGELII ROOT, AND TURPENTINE OIL) TABLET [MEDINATURA INC] 2 Legacy NDC, 2 package rows 20230420_4d2184f0-30f3-4d8c-b51e-1a879be25640.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 62795-9004-2 62795900402 1 BOTTLE in 1 CARTON (62795-9004-2) > 100 TABLET in 1 BOTTLE 1 bottle 2022-02-21 0000-00-00 No No Current