Antibacterial Hand Cleanser, Non-Alcohol

Product NDC
75866-001
11-digit product format
758660001
Labeler code
75866
Product ID
75866-001_c8d3457f-68cb-43ce-9a38-0a5bccae280f
Type
HUMAN OTC DRUG
Nonproprietary name
BENZALKONIUM CHLORIDE
Dosage form
GEL
Route
TOPICAL
Labeler
Beacon Promotions
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2010-12-29
Marketing end
0000-00-00
Substance
BENZALKONIUM CHLORIDE
Active strength
1 mg/mL
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75866-001-05Antibacterial Hand Cleanser, Non-Alcohol5 mL in 1 BOTTLEGEL55
75866-001-10Antibacterial Hand Cleanser, Non-Alcohol10 mL in 1 BOTTLEGEL105
75866-001-20Antibacterial Hand Cleanser, Non-Alcohol20 mL in 1 BOTTLEGEL205

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75866-001ANTIBACTERIAL HAND CLEANSER, NON-ALCOHOL (BENZALKONIUM CHLORIDE) GEL [BEACON PROMOTIONS]5Legacy NDC, 3 package rows20140222_260057a7-9e8a-4901-bbea-5fdc039fa27f.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049228benzalkonium chloride 0.1 % Topical GelPSN260057a7-9e8a-4901-bbea-5fdc039fa27f5
1049228benzalkonium chloride 0.001 MG/MG Topical GelSCD260057a7-9e8a-4901-bbea-5fdc039fa27f5
1049228benzalkonium chloride 0.1 % Topical GelSY260057a7-9e8a-4901-bbea-5fdc039fa27f5

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
75866-001-05758660001055 mL in 1 BOTTLE5 mlHistorical
75866-001-107586600011010 mL in 1 BOTTLE10 mlHistorical
75866-001-207586600012020 mL in 1 BOTTLE20 mlHistorical