SCOTT FOAM HAND SANITIZER

Product NDC
55118-664
11-digit product format
551180664
Labeler code
55118
Product ID
55118-664_270045e1-eb97-4a6f-a28c-2b6391a1088c
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
2018-11-16
Substance
BENZALKONIUM CHLORIDE
Active strength
1.3 mg/1000mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
SCOTT FOAM HAND SANITIZER
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE1.3 mg/1000mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiF5UM2KM3W7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55118-664-10SCOTT FOAM HAND SANITIZER1000 mL in 1 BOTTLESOLUTION10008
55118-664-12SCOTT FOAM HAND SANITIZER1200 mL in 1 BOTTLESOLUTION12008
55118-664-63SCOTT FOAM HAND SANITIZER6 in 1 CARTONSOLUTION68
55118-664-65SCOTT FOAM HAND SANITIZER2 in 1 CARTONSOLUTION28

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55118-664SCOTT FOAM HAND SANITIZER (BENZALKONIUM CHLORIDE) SOLUTION [KIMBERLY-CLARK]6Current NDC, Legacy NDC, 4 package rows20241215_11234f21-04e4-4b16-88c3-51968a1cedca.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55118-664-10551180664101000 mL in 1 BOTTLE1000 mlHistorical
55118-664-12551180664121200 mL in 1 BOTTLE1200 mlHistorical
55118-664-63551180664636 BOTTLE in 1 CARTON (55118-664-63) / 1000 mL in 1 BOTTLE (55118-664-10) 6 bottle2018-11-160000-00-00NoNoCurrent
55118-664-65551180664652 BOTTLE in 1 CARTON (55118-664-65) / 1200 mL in 1 BOTTLE (55118-664-12) 2 bottle2018-11-160000-00-00NoNoCurrent