FDA.reportPublic FDA data

Dr Lift Antibacterial

Product NDC
68062-2243
11-digit product format
680622243
Labeler code
68062
Product ID
68062-2243_40d7c6af-e655-d3e5-e063-6394a90af01c
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium Chloride
Dosage form
LOTION
Route
TOPICAL
Labeler
Spa de Soleil
Application
M003
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-09-17
Substance
BENZALKONIUM CHLORIDE
Active strength
.156 mg/120mg
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
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE.156 mg/120mg

Harmonized Identifiers#

Field, Values table
FieldValues
UniiF5UM2KM3W7
Rxcui1046442

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68062-2243-12025-01-30C16284748780-12cef2736-89bd-d83d-e063-dadaa90ab31fDr Lift Antibacterial Body Lotion
68062-2243-12025-01-30C16284748780-12cef2736-89bd-d83d-e063-dadaa90ab31fDr Lift Antibacterial Body Lotion

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68062-2243-1Dr Lift Antibacterial120 mg in 1 BOTTLELOTION1202
68062-2243-2Dr Lift Antibacterial100 mg in 1 BOTTLELOTION1002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68062-2243DR LIFT ANTIBACTERIAL (BENZALKONIUM CHLORIDE) LOTION [SPA DE SOLEIL]1Current NDC, Legacy NDC, 2 package rows20200918_af89675e-e66f-0922-e053-2995a90ab9d2.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1046442benzalkonium chloride 0.13 % Topical LotionPSNaf89675e-e66f-0922-e053-2995a90ab9d22
1046442benzalkonium chloride 1.3 MG/ML Topical LotionSCDaf89675e-e66f-0922-e053-2995a90ab9d22
1046442benzalkonium chloride 0.13 % Topical LotionSYaf89675e-e66f-0922-e053-2995a90ab9d22

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68062-2243-168062224301120 mg in 1 BOTTLE (68062-2243-1) 120 mg2020-09-170000-00-00NoNoCurrent
68062-2243-268062224302100 mg in 1 BOTTLE (68062-2243-2) 100 mg2025-10-10NoNoCurrent