BYD Hand Sanitizer Universal

Product NDC
73818-012
Requested package NDC
73818-012-01
11-digit product format
738180012
Labeler code
73818
Product ID
73818-012_a1c56494-a7b5-93b8-e053-2a95a90ac6b5
Type
HUMAN OTC DRUG
Nonproprietary name
alcohol
Dosage form
GEL
Route
TOPICAL
Labeler
Shanwei BYD Industry Co.,Ltd.
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-03-26
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

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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage73818-01273818-012-01DDiscontinued by firm2026-07-31

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73818-012-0173818001201500 mL in 1 POUCH (73818-012-01) 500 ml2020-03-260000-00-00NoNoCurrent