Home NDC 68428-134-01 Berberis Vulgaris Kit Refill
Product NDC 68428-134
Requested package NDC 68428-134-01
11-digit product format 684280134
Labeler code 68428
Product ID 68428-134_997c3ee0-a5b7-162a-e053-2995a90a6424
Type HUMAN OTC DRUG
Nonproprietary name BERBERIS VULGARIS ROOT BARK
Dosage form PELLET
Route ORAL
Labeler Washington Homeopathic Products
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-10-09
Marketing end 0000-00-00
Substance BERBERIS VULGARIS ROOT BARK
Active strength 30 [hp_C]/1
NDC exclude flag No
Listing certified through 2020-12-31
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 · 10 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…2019-12-08 06:16 UTC · source 2019-12-05 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
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 68428-134-01 30C Homeopathic Remedy Kit 750 in 1 VIAL, GLASS PELLET 750 30 [hp_C] 2 68428-134-01 Complete 30C/200C Homeopathic Kit 750 in 1 VIAL, GLASS PELLET 750 30 [hp_C] 2 68428-134-01 Berberis Vulgaris Kit Refill 750 in 1 VIAL, GLASS PELLET 750 2
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68428-134 BERBERIS VULGARIS KIT REFILL (BERBERIS VULGARIS ROOT BARK) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS] 2 Legacy NDC, 1 package rows 20191214_c5f16738-c53e-4f1b-9ebc-cd8034a88914.zip 68428-134 30C HOMEOPATHIC REMEDY KIT (50 REMEDY KIT) KIT [WASHINGTON HOMEOPATHIC PRODUCTS] 1 Legacy NDC 20240224_11e5ee81-1391-0dd3-e063-6294a90a5d0b.zip 68428-134 COMPLETE 30C/200C HOMEOPATHIC KIT (100 REMEDY KIT) KIT [WASHINGTON HOMEOPATHIC PRODUCTS] 1 Legacy NDC 20240516_16ecc94f-1001-983c-e063-6294a90a7b6c.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 68428-134-01 68428013401 750 PELLET in 1 VIAL, GLASS (68428-134-01) 750 pellet 2009-10-09 0000-00-00 No No Current