5257 Hand Sanitizer

Product NDC
76138-121
11-digit product format
761380121
Labeler code
76138
Product ID
76138-121_5d1cde54-e0c0-4665-8a41-1771387afeec
Type
HUMAN OTC DRUG
Nonproprietary name
ETHYL ALCOHOL
Dosage form
GEL
Route
TOPICAL
Labeler
Innovation Specialties
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2019-03-11
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
62 mL/100mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76138-121-037613801210330 mL in 1 BOTTLE (76138-121-03) 30 ml2019-03-110000-00-00NoNoCurrent