Home NDC 63083-1013-2 Poison Ivy/Oak
Product NDC 63083-1013
Requested package NDC 63083-1013-2
11-digit product format 630831013
Labeler code 63083
Product ID 63083-1013_885f50d0-117a-4b26-8394-2464c173d389
Type HUMAN OTC DRUG
Nonproprietary name Poison Ivy/Oak
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance AILANTHUS ALTISSIMA FRUIT; BEEF LIVER; CORTICOTROPIN; CROTON TIGLIUM SEED; ECHINACEA PURPUREA WHOLE; HISTAMINE DIHYDROCHLORIDE; SUS SCROFA ADRENAL GLAND; TOXICODENDRON DIVERSILOBUM LEAF; TOXICODENDRON PUBESCENS LEAF; URTICA DIOICA SUBSP. DIOICA LEAF; WOOD CREOSOTE; XEROPHYLLUM ASPHODELOIDES WHOLE
Active strength 6; 6; 6; 8; 2; 12; 6; 6; 6; 6; 12; 12 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes Adrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Meat Proteins [EXT], Non-Standardized Food Allergenic Extract [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 · 15 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Additional Listing Data#
Finished product Yes
Brand name base Poison Ivy/Oak
Brand name suffix 1013
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ECHINACEA PURPUREA WHOLE 2 [hp_X]/59mL SUS SCROFA ADRENAL GLAND 6 [hp_X]/59mL CORTICOTROPIN 6 [hp_X]/59mL BEEF LIVER 6 [hp_X]/59mL CROTON TIGLIUM SEED 8 [hp_X]/59mL HISTAMINE DIHYDROCHLORIDE 12 [hp_X]/59mL WOOD CREOSOTE 12 [hp_X]/59mL XEROPHYLLUM ASPHODELOIDES WHOLE 12 [hp_X]/59mL TOXICODENDRON DIVERSILOBUM LEAF 6 [hp_X]/59mL TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/59mL URTICA DIOICA SUBSP. DIOICA LEAF 6 [hp_X]/59mL AILANTHUS ALTISSIMA FRUIT 6 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 12 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# Effective, Related label table Effective Related label 2026-01-09 AOAK 2026-01-09 AOAK 2024-01-30 AOAK 2024-01-30 AOAK
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-1013-2 Poison Ivy/Oak1013 59 mL in 1 BOTTLE, DROPPER LIQUID 59 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63083-1013 POISON IVY/OAK 1013 (POISON IVY/OAK) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220201_a75d1f82-703b-48a3-a6a2-a7ed1cdde0af.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 63083-1013-2 63083101302 59 mL in 1 BOTTLE, DROPPER (63083-1013-2) 59 ml 1985-08-15 0000-00-00 No No Current