FDA.reportPublic FDA data

Foaming Antibacterial Handsoap

Product NDC
68041-512
11-digit product format
680410512
Labeler code
68041
Product ID
68041-512_217f951b-d438-4d3e-aa24-4b820926caa1
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium chloride
Dosage form
LIQUID
Route
TOPICAL
Labeler
Chemcor Chemical Corporation
Application
M
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-07-15
Substance
BENZALKONIUM CHLORIDE
Active strength
.0013 mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Foaming Antibacterial Handsoap
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE.0013 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiF5UM2KM3W7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68041-512-01Foaming Antibacterial Handsoap3780 mL in 1 BOTTLELIQUID37808
68041-512-55Foaming Antibacterial Handsoap207900 mL in 1 DRUMLIQUID2079008

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68041-512FOAMING ANTIBACTERIAL HANDSOAP (BENZALKONIUM CHLORIDE) LIQUID [CHEMCOR CHEMICAL CORPORATION]7Current NDC, Legacy NDC, 2 package rows20241212_eed9b007-0dc1-4954-891f-a7a042e763aa.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68041-512-01680410512013780 mL in 1 BOTTLE (68041-512-01) 3780 ml2020-07-150000-00-00NoNoCurrent
68041-512-5568041051255207900 mL in 1 DRUM (68041-512-55) 207900 ml2020-07-15NoNoHistorical