DayClear Hand Sanitizer

Product NDC
58809-225
11-digit product format
588090225
Labeler code
58809
Product ID
58809-225_a3e960c9-c5cf-1d1c-e053-2a95a90afb85
Type
HUMAN OTC DRUG
Nonproprietary name
Ethyl Alcohol
Dosage form
GEL
Route
TOPICAL
Labeler
GM Pharmaceuticals, INC
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-04-01
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
1 mL/mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58809-225-025880902250259 mL in 1 BOTTLE (58809-225-02) 59 ml2020-04-010000-00-00NoNoCurrent
58809-225-0858809022508237 mL in 1 BOTTLE (58809-225-08) 237 ml2020-04-010000-00-00NoNoCurrent
58809-225-1258809022512355 mL in 1 BOTTLE (58809-225-12) 355 ml2020-04-010000-00-00NoNoCurrent
58809-225-3258809022532946 mL in 1 BOTTLE (58809-225-32) 946 ml2020-04-010000-00-00NoNoCurrent