BOREL ANTISEPTIC HAND SANITIZER

Product NDC
81126-020
11-digit product format
811260020
Labeler code
81126
Product ID
81126-020_a7fbba98-d780-47eb-8e77-fe782ddeeaf2
Type
HUMAN OTC DRUG
Nonproprietary name
Ethyl alcohol
Dosage form
LIQUID
Route
TOPICAL
Labeler
Eti Maden Isletmeleri Genel Mudurlugu
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-12-20
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
80 g/100mL
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 · 4 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct81126-020DDiscontinued by firm2026-10-16
excluded packagepackage81126-02081126-020-01DDiscontinued by firm2026-10-16
excluded packagepackage81126-02081126-020-02DDiscontinued by firm2026-10-16
excluded packagepackage81126-02081126-020-03DDiscontinued by firm2026-10-16

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 8 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage81126-020-02d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage81126-020-03d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage81126-020-01d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage81126-020-02f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage81126-020-03f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage81126-020-01f5e01cc5f278…a2eaf40c39c3…

Reported adverse events (FAERS/openFDA)#

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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
81126-020-0181126002001100 mL in 1 BOTTLE, SPRAY (81126-020-01) 100 ml2020-12-200000-00-00NoNoCurrent
81126-020-02811260020021000 mL in 1 BOTTLE (81126-020-02) 1000 ml2020-12-200000-00-00NoNoCurrent
81126-020-03811260020035000 mL in 1 JUG (81126-020-03) 5000 ml2020-12-200000-00-00NoNoCurrent