vanilla frosting scent hand sanitizer

Product NDC
74177-036
11-digit product format
741770036
Labeler code
74177
Product ID
74177-036_0897b5ff-caa2-5ed5-e063-6294a90a92ee
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
GEL
Route
TOPICAL
Labeler
K7 DESIGN GROUP INC
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-06-18
Substance
ALCOHOL
Active strength
.62 mL/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
vanilla frosting scent hand sanitizer
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL.62 mL/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii3K9958V90M
Rxcui581660

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74177-036-00vanilla frosting scent hand sanitizer30 mL in 1 BOTTLEGEL302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74177-036VANILLA FROSTING SCENT HAND SANITIZER (ALCOHOL) GEL [K7 DESIGN GROUP INC]2Current NDC, Legacy NDC, 1 package rows20231026_5960a9fc-3263-4881-9724-0575c4be3192.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
581660ethanol 62 % Topical GelPSN5960a9fc-3263-4881-9724-0575c4be31922
581660ethanol 0.62 ML/ML Topical GelSCD5960a9fc-3263-4881-9724-0575c4be31922
581660ethanol 62 % Topical GelSY5960a9fc-3263-4881-9724-0575c4be31922

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
74177-036-007417700360030 mL in 1 BOTTLE (74177-036-00) 30 ml2020-06-180000-00-00NoNoCurrent