Home NDC 77665-001 bolor sanitizing hand wipes
Product NDC 77665-001
11-digit product format 776650001
Labeler code 77665
Product ID 77665-001_3451ab76-6cc7-f269-e063-6294a90a4b92
Type HUMAN OTC DRUG
Nonproprietary name bolor sanitizing hand wipes
Dosage form SOLUTION
Route TOPICAL
Labeler Guangzhou Baihua Co., Ltd
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2025-04-01
Substance BENZALKONIUM CHLORIDE
Active strength 12 mg/100mg
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base bolor sanitizing hand wipes
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE 12 mg/100mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination F5UM2KM3W7 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 77665-001-01 bolor sanitizing hand wipes 100 mg in 1 PACKET SOLUTION 100 2 77665-001-02 bolor sanitizing hand wipes 60 in 1 PACKET SOLUTION 60 2 77665-001-03 bolor sanitizing hand wipes 100 mg in 1 PACKET SOLUTION 100 2 77665-001-04 bolor sanitizing hand wipes 30 in 1 PACKET SOLUTION 30 2 77665-001-05 bolor sanitizing hand wipes 100 mg in 1 PACKET SOLUTION 100 2 77665-001-06 bolor sanitizing hand wipes 10 in 1 PACKET SOLUTION 10 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 77665-001 BOLOR SANITIZING HAND WIPES SOLUTION [GUANGZHOU BAIHUA CO., LTD] 2 Current NDC, 6 package rows 20250506_33dbe9e3-4335-ada1-e063-6294a90ad2f5.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 Sample Exclude flag Status 77665-001-01 77665000101 100 mg in 1 PACKET 100 mg Historical 77665-001-02 77665000102 60 PACKET in 1 PACKET (77665-001-02) / 100 mg in 1 PACKET (77665-001-01) 60 packet 2025-04-01 No No Current 77665-001-03 77665000103 100 mg in 1 PACKET 100 mg Historical 77665-001-04 77665000104 30 PACKET in 1 PACKET (77665-001-04) / 100 mg in 1 PACKET (77665-001-03) 30 packet 2025-04-01 No No Current 77665-001-05 77665000105 100 mg in 1 PACKET 100 mg Historical 77665-001-06 77665000106 10 PACKET in 1 PACKET (77665-001-06) / 100 mg in 1 PACKET (77665-001-05) 10 packet 2025-04-01 No No Current