CONTACT ALLERGY ANTIGEN

Product NDC
43406-0115
Requested package NDC
43406-0115-1
11-digit product format
434060115
Labeler code
43406
Product ID
43406-0115_33da2e7d-edeb-4d1f-8761-d5be86cb3f69
Type
HUMAN OTC DRUG
Nonproprietary name
Toxicodendron Diversilobum Leaf, Toxicodendron Pubescens Leaf, Toxicodendron Vernix Leafy Twig, Urtica Dioica, Semecarpus Anacardium Juice, Graphite, Daphne Mezereum Bark, Urtica Urens, Xerophyllum Asphodeloides
Dosage form
LIQUID
Route
ORAL
Labeler
Natural Creations, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2010-01-01
Marketing end
0000-00-00
Substance
TOXICODENDRON DIVERSILOBUM LEAF; TOXICODENDRON PUBESCENS LEAF; TOXICODENDRON VERNIX LEAFY TWIG; URTICA DIOICA; SEMECARPUS ANACARDIUM FRUIT; GRAPHITE; DAPHNE MEZEREUM BARK; URTICA URENS; XEROPHYLLUM ASPHODELOIDES
Active strength
30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage43406-011543406-0115-1IInactivated by FDA2026-10-05

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 · 19 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05IInactivated by FDAd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26IInactivated by FDAf5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31IInactivated by FDA2ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28IInactivated by FDAa1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21IInactivated by FDAcfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10IInactivated by FDAcdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31IInactivated by FDA302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20IInactivated by FDAed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10IInactivated by FDA0efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08IInactivated by FDAad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03IInactivated by FDA367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09IInactivated by FDA557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-28IInactivated by FDA8af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14IInactivated by FDA834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-08IInactivated by FDA1332a3947898…d4bfe170f9cd…
2022-08-30 03:57 UTC · source 2022-08-29IInactivated by FDAfb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-08IInactivated by FDA86f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01IInactivated by FDAbd6a592717d7…303034d00443…
2019-12-08 06:16 UTC · source 2019-12-05EExcluded after deficient or non-compliant submission was not corrected110d247fa046…a55b01930146…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43406-0115-12022-01-28C16284748780-19d75b9d0-3583-f424-e053-dadaa90a57ceCONTACT ALLERGY ANTIGEN
43406-0115-12020-06-02C16284748780-19d75b9d0-3583-f424-e053-dadaa90a57ceCONTACT ALLERGY ANTIGEN
43406-0115-12020-01-31C16284748780-19d75b9d0-3583-f424-e053-dadaa90a57ceCONTACT ALLERGY ANTIGEN

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43406-0115-1CONTACT ALLERGY ANTIGEN30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43406-0115CONTACT ALLERGY ANTIGEN (TOXICODENDRON DIVERSILOBUM LEAF, TOXICODENDRON PUBESCENS LEAF, TOXICODENDRON VERNIX LEAFY TWIG, URTICA DIOICA, SEMECARPUS ANACARDIUM JUICE, GRAPHITE, DAPHNE MEZEREUM BARK, URTICA URENS, XEROPHYLLUM ASPHODELOIDES) LIQUID [NATURAL CREATIONS, INC.]2Legacy NDC, 1 package rows20200527_e17a8715-5e94-4d92-833f-9fb80f69abb7.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43406-0115-14340601150130 mL in 1 BOTTLE, DROPPER (43406-0115-1) 30 ml2010-01-010000-00-00NoNoCurrent