FDA.reportPublic FDA data

BYD Hand Sanitizer Universal

Product NDC
73818-015
Requested package NDC
73818-015-04
11-digit product format
738180015
Labeler code
73818
Product ID
73818-015_a27d6185-e416-2774-e053-2a95a90a972f
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
2020-04-04
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 packagepackage73818-01573818-015-04DDiscontinued by firm2026-07-31

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73818-015-042023-07-05C16284748780-1d6a99b39-39d3-a426-e053-dadaa90af4c2a27d6c02-cf51-f233-e053-2995a90a2228
73818-015-042022-01-28C16284748780-1d6a99b39-39d3-a426-e053-dadaa90af4c2a27d6c02-cf51-f233-e053-2995a90a2228

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73818-015-0473818001504236 mL in 1 BOTTLE, DISPENSING (73818-015-04) 236 ml2020-04-040000-00-00NoNoCurrent