Home NDC 73076-502 Homwis Eczema Relief
Product NDC 73076-502
11-digit product format 730760502
Labeler code 73076
Product ID 73076-502_49f926b7-7346-a2fe-e063-6294a90af812
Type HUMAN OTC DRUG
Nonproprietary name Homwis Eczema Relief
Dosage form SOAP
Route TOPICAL
Labeler Shenzhen Ishan Technology Co., Ltd
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2025-02-01
Substance MELALEUCA ALTERNIFOLIA LEAF
Active strength 1 g/100g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Homwis Eczema Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MELALEUCA ALTERNIFOLIA LEAF 1 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G43C57162K Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73076-502-02 Homwis Eczema Relief 100 g in 1 BOX SOAP 100 1
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 Sample Exclude flag Status 73076-502-02 73076050202 100 g in 1 BOX (73076-502-02) 100 g 2025-02-01 No No Current