Home NDC 66096-192 Eczema Relief
Product NDC 66096-192
11-digit product format 660960192
Labeler code 66096
Product ID 66096-192_d44acb83-411f-5445-e053-2995a90a6760
Type HUMAN OTC DRUG
Nonproprietary name Arsenicum Iodatum, Kali Bromatum, Kali Muriaticum, Natrum Bromatum, Niccolum Sulphuricum, Sulphur Iodatum, Viola Tricolor, Zincum Bromatum.
Dosage form LIQUID
Route ORAL
Labeler OHM PHARMA INC.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-05-22
Substance ARSENIC TRIIODIDE; NICKEL SULFATE HEXAHYDRATE; POTASSIUM BROMIDE; POTASSIUM CHLORIDE; SODIUM BROMIDE; SULFUR IODIDE; VIOLA TRICOLOR; ZINC BROMIDE
Active strength 8; 5; 4; 4; 4; 14; 12; 6 [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 Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], 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 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Eczema Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARSENIC TRIIODIDE 8 [hp_X]/59mL POTASSIUM BROMIDE 5 [hp_X]/59mL POTASSIUM CHLORIDE 4 [hp_X]/59mL SODIUM BROMIDE 4 [hp_X]/59mL NICKEL SULFATE HEXAHYDRATE 4 [hp_X]/59mL SULFUR IODIDE 14 [hp_X]/59mL VIOLA TRICOLOR 12 [hp_X]/59mL ZINC BROMIDE 6 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 8 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 66096-192-05 Eczema Relief 59 mL in 1 PACKAGE LIQUID 59 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 66096-192 ECZEMA RELIEF (ARSENICUM IODATUM, KALI BROMATUM, KALI MURIATICUM, NATRUM BROMATUM, NICCOLUM SULPHURICUM, SULPHUR IODATUM, VIOLA TRICOLOR, ZINCUM BROMATUM.) LIQUID [OHM PHARMA INC.] 4 Current NDC, Legacy NDC, 1 package rows 20211230_92077b39-ed44-4d73-865f-0ec83e994940.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.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Eczema Relief ARSENICUM IODATUM, KALI BROMATUM, KALI MURIATICUM, NATRUM BROMATUM, NICCOLUM SULPHURICUM, SULPHUR IODATUM, VIOLA TRICOLOR, ZINCUM BROMATUM. OHM PHARMA INC. 92077b39-ed44-4d73-865f-0ec83e994940 2021-12-29 Warnings Exact identifier ndc (product): 66096-192
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 66096-192-05 66096019205 59 mL in 1 PACKAGE (66096-192-05) 59 ml 2015-05-22 0000-00-00 No No Current