Anti-BacterialHandSpray

Product NDC
62670-6887
11-digit product format
626706887
Labeler code
62670
Product ID
62670-6887_4c11366c-1491-70c2-e063-6294a90a8e9f
Type
HUMAN OTC DRUG
Nonproprietary name
Alcohol
Dosage form
SPRAY
Route
TOPICAL
Labeler
Bath & Body Works, Inc.
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-02-10
Substance
ALCOHOL
Active strength
72 mL/100mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Anti-BacterialHandSpray
Brand name suffix
Sweet Kiwi and Starfruit
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL72 mL/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii3K9958V90M
Rxcui1425407

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62670-6887-2Anti-BacterialHandSpraySweet Kiwi and Starfruit29 mL in 1 BOTTLE, SPRAYSPRAY292

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1425407ethanol 72 % Topical SprayPSN38d5d1c4-7f5b-45af-e063-6394a90a9c472
1425407ethanol 0.72 ML/ML Topical SpraySCD38d5d1c4-7f5b-45af-e063-6394a90a9c472
1425407ethanol 72 % Topical SpraySY38d5d1c4-7f5b-45af-e063-6394a90a9c472

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
62670-6887-26267068870229 mL in 1 BOTTLE, SPRAY (62670-6887-2) 29 ml2025-02-10NoNoHistorical