Home NDC 55118-701 KLEENEX Foam Hand Sanitizer
Product NDC 55118-701
11-digit product format 551180701
Labeler code 55118
Product ID 55118-701_30f0ed99-94db-4881-8061-ec3b50c62b64
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride
Dosage form SOLUTION
Route TOPICAL
Labeler Kimberly-Clark
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-09-01
Substance BENZALKONIUM CHLORIDE
Active strength 1.3 mg/1000mL
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 KLEENEX Foam Hand Sanitizer
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE 1.3 mg/1000mL
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 55118-701-10 KLEENEX Foam Hand Sanitizer 1000 mL in 1 CARTRIDGE SOLUTION 1000 8 55118-701-11 KLEENEX Foam Hand Sanitizer 45 mL in 1 BOTTLE, PUMP SOLUTION 45 8 55118-701-12 KLEENEX Foam Hand Sanitizer 1200 mL in 1 CARTRIDGE SOLUTION 1200 8 55118-701-18 KLEENEX Foam Hand Sanitizer 532 mL in 1 BOTTLE, PUMP SOLUTION 532 8 55118-701-64 KLEENEX Foam Hand Sanitizer 24 in 1 CARTON SOLUTION 24 8 55118-701-67 KLEENEX Foam Hand Sanitizer 4 in 1 CARTON SOLUTION 4 8 55118-701-99 KLEENEX Foam Hand Sanitizer 473 mL in 1 BOTTLE, PUMP SOLUTION 473 8
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55118-701 KLEENEX FOAM HAND SANITIZER (BENZALKONIUM CHLORIDE) SOLUTION [KIMBERLY-CLARK] 6 Current NDC, Legacy NDC, 7 package rows 20241215_1fa77ae2-b652-463d-8943-d338c591226e.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 9 of 115 · 2,286 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 55118-701-10 55118070110 1000 mL in 1 CARTRIDGE (55118-701-10) 1000 ml 2015-09-01 0000-00-00 No No Current 55118-701-11 55118070111 45 mL in 1 BOTTLE, PUMP 45 ml Historical 55118-701-12 55118070112 1200 mL in 1 CARTRIDGE (55118-701-12) 1200 ml 2015-09-01 0000-00-00 No No Current 55118-701-18 55118070118 532 mL in 1 BOTTLE, PUMP 532 ml Historical 55118-701-64 55118070164 24 BOTTLE, PUMP in 1 CARTON (55118-701-64) / 45 mL in 1 BOTTLE, PUMP (55118-701-11) 2015-09-01 0000-00-00 No No Current 55118-701-67 55118070167 4 BOTTLE, PUMP in 1 CARTON (55118-701-67) / 532 mL in 1 BOTTLE, PUMP (55118-701-18) 2015-09-01 0000-00-00 No No Current 55118-701-99 55118070199 473 mL in 1 BOTTLE, PUMP (55118-701-99) 473 ml 2015-09-01 0000-00-00 No No Current