Hand Sanitizer

Product NDC
23400-760
11-digit product format
234000760
Labeler code
23400
Product ID
23400-760_b830f120-5283-f3d0-e053-2995a90a4158
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
GEL
Route
TOPICAL
Labeler
U.S. Borax Inc.
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-03-30
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
80 mL/100mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
23400-760-012022-07-29C16284748780-1e4f33bdf-a9a9-d8a0-e053-dadaa90a6e4eHand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
23400-760-01Hand Sanitizer3785.41 mL in 1 BOTTLE, PUMPGEL3785.415

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
23400-760HAND SANITIZER (ALCOHOL) GEL [U.S. BORAX INC.]5Legacy NDC, 1 package rows20210106_a229ae5f-2b08-9ecd-e053-2a95a90a756a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
23400-760-01234000760013785.41 mL in 1 BOTTLE, PUMP (23400-760-01) 3785.41 ml2020-03-300000-00-00NoNoCurrent