Home NDC 84449-009-01 Novo Wipe
Product NDC 84449-009
Requested package NDC 84449-009-01
11-digit product format 844490009
Labeler code 84449
Product ID 84449-009_545c6386-139f-cb9b-e063-6394a90a0456
Type HUMAN OTC DRUG
Nonproprietary name Novo Wipe
Dosage form PATCH
Route TOPICAL
Labeler SHENZHEN BENLIJU BIO-TECH CO.,LTD
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-16
Substance ALCOHOL
Active strength .25 g/g
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 Novo Wipe
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL .25 g/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3K9958V90M Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 70 of 114 · 2,277 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84449-009-01 84449000901 1 g in 1 PATCH (84449-009-01) 1 g 2026-06-16 No No Current