Anti-BacterialHandSpray

Product NDC
62670-6799
11-digit product format
626706799
Labeler code
62670
Product ID
62670-6799_29a3af99-8187-9ec6-e063-6294a90ab842
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
2024-11-18
Marketing end
2027-11-18
Substance
ALCOHOL
Active strength
72 mL/100mL
NDC exclude flag
No
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
3K9958V90MALCOHOL64-17-5ALCOHOL

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
62670-6799-06267067990029 mL in 1 BOTTLE, SPRAY (62670-6799-0) 29 ml2024-11-182027-11-18NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
1oz ABHS Boardwalk Vanilla ConeBath & Body Works, Inc. | KDC US Holdings, Inc.2024-12-19HUMAN OTC DRUG LABEL1