Home NDC 63083-2136-2 Wet Eczema Drops
Product NDC 63083-2136
Requested package NDC 63083-2136-2
11-digit product format 630832136
Labeler code 63083
Product ID 63083-2136_0597f5dc-11b0-423c-b516-3fea39591f30
Type HUMAN OTC DRUG
Nonproprietary name Wet Eczema Drops
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance ARSENIC TRIIODIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CLEMATIS RECTA FLOWERING TOP; CALCIUM SULFIDE; POTASSIUM SULFATE; DAPHNE MEZEREUM BARK; LIQUID PETROLEUM; TOXICODENDRON PUBESCENS LEAF; SULFUR; ARSENIC TRIOXIDE; GRAPHITE
Active strength 6; 6; 6; 6; 6; 6; 6; 6; 8; 9; 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
Pharmacologic classes Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [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…
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 Wet Eczema Drops
Brand name suffix 2136
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARSENIC TRIIODIDE 6 [hp_X]/59mL OYSTER SHELL CALCIUM CARBONATE, CRUDE 6 [hp_X]/59mL CLEMATIS RECTA FLOWERING TOP 6 [hp_X]/59mL CALCIUM SULFIDE 6 [hp_X]/59mL POTASSIUM SULFATE 6 [hp_X]/59mL DAPHNE MEZEREUM BARK 6 [hp_X]/59mL LIQUID PETROLEUM 6 [hp_X]/59mL TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/59mL SULFUR 8 [hp_X]/59mL ARSENIC TRIOXIDE 9 [hp_X]/59mL GRAPHITE 12 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 11 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 2026-01-08 C136 2026-01-08 C136 2024-01-30 C136 2024-01-30 C136
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2136-2 Wet Eczema Drops2136 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 63083-2136 WET ECZEMA DROPS 2136 (WET ECZEMA DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220216_28f08a29-9b1a-4579-a56f-4cab7cdcfcb6.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 63083-2136-2 63083213602 59 mL in 1 BOTTLE, DROPPER (63083-2136-2) 59 ml 1985-08-15 0000-00-00 No No Current