Home NDC 73076-504 HOMWIS Cream
Product NDC 73076-504
11-digit product format 730760504
Labeler code 73076
Product ID 73076-504_5626af5c-ed2f-c0a7-e063-6394a90a4596
Type HUMAN OTC DRUG
Nonproprietary name HOMWIS Cream
Dosage form OINTMENT
Route TOPICAL
Labeler Shenzhen Ishan Technology Co., Ltd
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2025-01-01
Substance PETROLATUM
Active strength .196 g/20g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 HOMWIS Cream
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PETROLATUM .196 g/20g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4T6H12BN9U 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 73076-504-05 HOMWIS Cream 50 g in 1 JAR OINTMENT 50 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 73076-504-02 73076050402 45 g in 1 JAR (73076-504-02) 45 g 2025-01-01 No No Current 73076-504-03 73076050403 50 g in 1 JAR (73076-504-03) 50 g 2025-01-01 No No Current 73076-504-05 73076050405 50 g in 1 JAR 50 g Historical