Home NDC 83829-005-01 Eco Bandage SAND
Product NDC 83829-005
Requested package NDC 83829-005-01
11-digit product format 838290005
Labeler code 83829
Product ID 83829-005_4c5cbca4-1abd-2db4-e063-6294a90a2a49
Type HUMAN OTC DRUG
Nonproprietary name Benzethonium Chloride
Dosage form LIQUID
Route TOPICAL
Labeler Eco Bandage LLC
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-03-05
Substance BENZETHONIUM CHLORIDE
Active strength .2 g/100mL
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 Eco Bandage SAND
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZETHONIUM CHLORIDE .2 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination PH41D05744 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 83829-005-01 Eco Bandage SAND 10 mL in 1 BOTTLE LIQUID 10 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 85 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 83829-005-01 83829000501 10 mL in 1 BOTTLE (83829-005-01) 10 ml 2026-03-05 No No Current