Anti-BacterialHandSpray

Product NDC
62670-6796
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
Substance
ALCOHOL
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
62670-6796-029 mL in 1 BOTTLE, SPRAY (62670-6796-0) 2024-11-182027-11-18NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
1oz ABHS Sun Washed CitrusBath & Body Works, Inc. | KDC US Holdings, Inc.2024-12-19HUMAN OTC DRUG LABEL1