SPARKLING CRANBERRY HAND SANITIZER

Product NDC
11673-782
11-digit product format
116730782
Labeler code
11673
Product ID
11673-782_0899102b-2f94-acce-e063-6394a90a2256
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
GEL
Route
TOPICAL
Labeler
Target Corporation
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-08-28
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
SPARKLING CRANBERRY 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
11673-782-00SPARKLING CRANBERRY HAND SANITIZER30 mL in 1 BOTTLEGEL302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-782SPARKLING CRANBERRY HAND SANITIZER (ALCOHOL) GEL [TARGET CORPORATION]2Current NDC, Legacy NDC, 1 package rows20231026_7ca828e8-ff43-4e4c-8e8c-d760a0f0c222.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
581660ethanol 62 % Topical GelPSN7ca828e8-ff43-4e4c-8e8c-d760a0f0c2222
581660ethanol 0.62 ML/ML Topical GelSCD7ca828e8-ff43-4e4c-8e8c-d760a0f0c2222
581660ethanol 62 % Topical GelSY7ca828e8-ff43-4e4c-8e8c-d760a0f0c2222

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11673-782-001167307820030 mL in 1 BOTTLE (11673-782-00) 30 ml2020-08-280000-00-00NoNoCurrent