Home NDC 50718-0012 Calm Eczema Therapy Wash
Product NDC 50718-0012
11-digit product format 507180012
Labeler code 50718
Product ID 50718-0012_de207320-7cf9-4c1a-9f60-c55e0a63885b
Type HUMAN OTC DRUG
Nonproprietary name Sulphur 12X
Dosage form LIQUID
Route TOPICAL
Labeler Kamedis
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2018-01-01
Substance SULFUR
Active strength 12 [hp_X]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Calm Eczema Therapy Wash
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SULFUR 12 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 70FD1KFU70 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 50718-0012-1 Calm Eczema Therapy Wash 200 mL in 1 TUBE LIQUID 200 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50718-0012 CALM ECZEMA THERAPY WASH (SULPHUR 12X) LIQUID [KAMEDIS] 4 Current NDC, Legacy NDC, 1 package rows 20240213_38a3495e-6872-4cb8-bab7-1c93e1470e2c.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 50718-0012-1 50718001201 200 mL in 1 TUBE (50718-0012-1) 200 ml 2018-01-01 0000-00-00 No No Current