FDA.reportPublic FDA data

Kong HandiPOD

Product NDC
71427-213
11-digit product format
714270213
Labeler code
71427
Product ID
71427-213_4f18b7b6-ff38-2cf3-e054-00144ff8d46c
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
GEL
Route
TOPICAL
Labeler
HANDIPOD LIMITED
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2017-05-09
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
700 mg/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct71427-213DDiscontinued by firm2026-07-31
excluded packagepackage71427-21371427-213-45DDiscontinued by firm2026-07-31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71427-213-457142702134545 mL in 1 BOTTLE (71427-213-45) 45 ml2017-05-090000-00-00NoNoCurrent