Home NDC 59555-401 I.C. Hand Sanitizer
Product NDC 59555-401
11-digit product format 595550401
Labeler code 59555
Product ID 59555-401_4615b07d-430b-4729-e063-6394a90a064b
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride
Dosage form AEROSOL, FOAM
Route TOPICAL
Labeler R&R Lotion, Inc.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-06-14
Substance BENZALKONIUM CHLORIDE
Active strength 1 mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 40 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 59555-401-11 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 59555-401-13 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 59555-401-12 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 59555-401-11 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 59555-401-13 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 59555-401-12 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 59555-401-11 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 59555-401-13 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 59555-401-12 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 59555-401-11 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 59555-401-13 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 59555-401-12 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 59555-401-11 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 59555-401-13 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 59555-401-12 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 59555-401-11 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 59555-401-13 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 59555-401-12 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 59555-401-11 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 59555-401-12 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 59555-401-13 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 59555-401-11 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 59555-401-12 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 59555-401-13 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 59555-401-11 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 59555-401-12 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 59555-401-13 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product I Inactivated by FDA 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 59555-401-11 I Inactivated by FDA 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 59555-401-13 I Inactivated by FDA 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 59555-401-12 I Inactivated by FDA 110d247fa046…a55b01930146…
Additional Listing Data#
Finished product Yes
Brand name base I.C. Hand Sanitizer
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE 1 mg/mL
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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1038799 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59555-401-04 I.C. Hand Sanitizer 59 mL in 1 BOTTLE, SPRAY AEROSOL, FOAM 59 6 59555-401-11 I.C. Hand Sanitizer 3785 mL in 1 BOTTLE, PUMP AEROSOL, FOAM 3785 6 59555-401-12 I.C. Hand Sanitizer 591 mL in 1 BOTTLE, PUMP AEROSOL, FOAM 591 6 59555-401-13 I.C. Hand Sanitizer 50 mL in 1 BOTTLE, PUMP AEROSOL, FOAM 50 6
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Benzalkonium Chloride ACTIVE INGREDIENT F5UM2KM3W7 I.C. HAND SANITIZER (BENZALKONIUM CHLORIDE) AEROSOL, FOAM [R&R LOTION, INC.] 1 Benzalkonium ACTIVE MOIETY 7N6JUD5X6Y I.C. HAND SANITIZER (BENZALKONIUM CHLORIDE) AEROSOL, FOAM [R&R LOTION, INC.] 1 Cetrimonium Chloride INACTIVE INGREDIENT UC9PE95IBP I.C. HAND SANITIZER (BENZALKONIUM CHLORIDE) AEROSOL, FOAM [R&R LOTION, INC.] 1 Citric Acid Monohydrate INACTIVE INGREDIENT 2968PHW8QP I.C. HAND SANITIZER (BENZALKONIUM CHLORIDE) AEROSOL, FOAM [R&R LOTION, INC.] 1 Dihydroxyethyl Cocamine Oxide INACTIVE INGREDIENT 8AR51R3BL5 I.C. HAND SANITIZER (BENZALKONIUM CHLORIDE) AEROSOL, FOAM [R&R LOTION, INC.] 1 Glycereth-17 Cocoate INACTIVE INGREDIENT 3057VPT0KC I.C. HAND SANITIZER (BENZALKONIUM CHLORIDE) AEROSOL, FOAM [R&R LOTION, INC.] 1 Laurtrimonium Chloride INACTIVE INGREDIENT A81MSI0FIC I.C. HAND SANITIZER (BENZALKONIUM CHLORIDE) AEROSOL, FOAM [R&R LOTION, INC.] 1 Water INACTIVE INGREDIENT 059QF0KO0R I.C. HAND SANITIZER (BENZALKONIUM CHLORIDE) AEROSOL, FOAM [R&R LOTION, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59555-401 I.C. HAND SANITIZER (BENZALKONIUM CHLORIDE) AEROSOL, FOAM [R&R LOTION, INC.] 3 Current NDC, Legacy NDC, 4 package rows 20220215_5361bb71-cc84-4a76-a0cf-2259a615baa4.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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 59555-401-04 59555040104 59 mL in 1 BOTTLE, SPRAY (59555-401-04) 59 ml 2014-06-15 No No Current 59555-401-11 59555040111 3785 mL in 1 BOTTLE, PUMP (59555-401-11) 3785 ml 2014-06-15 0000-00-00 No No Current 59555-401-12 59555040112 591 mL in 1 BOTTLE, PUMP (59555-401-12) 591 ml 2014-06-15 0000-00-00 No No Current 59555-401-13 59555040113 50 mL in 1 BOTTLE, PUMP (59555-401-13) 50 ml 2014-06-15 0000-00-00 No No Current