Dr Lift Antibacterial Hand Sanitizer

Product NDC
68062-2250
11-digit product format
680622250
Labeler code
68062
Product ID
68062-2250_436f3a5d-a6a3-615c-e063-6394a90abd10
Type
HUMAN OTC DRUG
Nonproprietary name
ethyl alcohol
Dosage form
GEL
Route
TOPICAL
Labeler
Spa de Soleil
Application
M003
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-07-29
Substance
ALCOHOL
Active strength
168 mL/240mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Dr Lift Antibacterial Hand Sanitizer
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL168 mL/240mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii3K9958V90M
Rxcui581662

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68062-2250-1Dr Lift Antibacterial Hand Sanitizer240 mL in 1 BOTTLE, PUMPGEL2403

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
581662ethanol 70 % Topical GelPSNaba006cd-18db-e42f-e053-2995a90a46073
581662ethanol 0.7 ML/ML Topical GelSCDaba006cd-18db-e42f-e053-2995a90a46073
581662ethanol 70 % Topical GelSYaba006cd-18db-e42f-e053-2995a90a46073
581662ethyl alcohol 70 % Topical GelSYaba006cd-18db-e42f-e053-2995a90a46073

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68062-2250-168062225001240 mL in 1 BOTTLE, PUMP (68062-2250-1) 240 ml2020-07-290000-00-00NoNoCurrent