Saninta Hand Sanitizing Gel

Product NDC
81351-002
11-digit product format
813510002
Labeler code
81351
Product ID
81351-002_ec1e0731-141a-5ad7-e053-2a95a90ace8b
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
LIQUID
Route
TOPICAL
Labeler
LL Pharma
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2021-03-15
Marketing end
0000-00-00
Substance
ISOPROPYL ALCOHOL
Active strength
1 mL/mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

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

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct81351-002DDiscontinued by firm2026-10-05
excluded packagepackage81351-00281351-002-01DDiscontinued by firm2026-10-05

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81351-002SANINTA HAND SANITIZING GEL (ALCOHOL) LIQUID [LL PHARMA]3Legacy NDC20231022_bd9f1acd-d681-9d13-e053-2a95a90a5868.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
81351-002-0181351000201118.3 mL in 1 PACKET (81351-002-01) 118.3 ml2021-03-150000-00-00NoNoCurrent