Home NDC 63083-2049-2 Poison Ivy Dermatosis Drops
Product NDC 63083-2049
Requested package NDC 63083-2049-2
11-digit product format 630832049
Labeler code 63083
Product ID 63083-2049_0add295d-4c20-42ff-96f2-031e177134ae
Type HUMAN OTC DRUG
Nonproprietary name Poison Ivy Dermatosis Drops
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance ECHINACEA PURPUREA WHOLE; GRINDELIA HIRSUTULA FLOWERING TOP; RANUNCULUS BULBOSUS WHOLE; URTICA URENS WHOLE; LYTTA VESICATORIA; DAPHNE MEZEREUM BARK; TOXICODENDRON PUBESCENS LEAF; XEROPHYLLUM ASPHODELOIDES WHOLE; CROTON TIGLIUM SEED
Active strength 2; 2; 3; 3; 4; 6; 6; 6; 8 [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
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…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Poison Ivy Dermatosis Drops
Brand name suffix 2049
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ECHINACEA PURPUREA WHOLE 2 [hp_X]/59mL GRINDELIA HIRSUTULA FLOWERING TOP 2 [hp_X]/59mL RANUNCULUS BULBOSUS WHOLE 3 [hp_X]/59mL URTICA URENS WHOLE 3 [hp_X]/59mL LYTTA VESICATORIA 4 [hp_X]/59mL DAPHNE MEZEREUM BARK 6 [hp_X]/59mL TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/59mL XEROPHYLLUM ASPHODELOIDES WHOLE 6 [hp_X]/59mL CROTON TIGLIUM SEED 8 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 9 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# Effective, Related label table Effective Related label 2026-01-08 C49 2026-01-08 C49 2024-01-30 C49 2024-01-30 C49
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2049-2 Poison Ivy Dermatosis Drops2049 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 63083-2049 POISON IVY DERMATOSIS DROPS 2049 (POISON IVY DERMATOSIS DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220216_ddf4a44f-a919-4bf7-b54d-241ac4c7ffd2.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 63083-2049-2 63083204902 59 mL in 1 BOTTLE, DROPPER (63083-2049-2) 59 ml 1985-08-15 0000-00-00 No No Current