FDA.reportPublic FDA data

Antibacterial Liquid Hand

Product NDC
51143-541
11-digit product format
511430541
Labeler code
51143
Product ID
51143-541_1412fee9-1ac0-472d-868c-542a1db339b8
Type
HUMAN OTC DRUG
Nonproprietary name
TRICLOSAN
Dosage form
LIQUID
Route
TOPICAL
Labeler
OnPoint, Inc
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2009-07-30
Marketing end
0000-00-00
Substance
TRICLOSAN
Active strength
0 kg/100L
NDC exclude flag
E
Listing certified through
2018-12-31
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 · 4 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct51143-541IInactivated by FDA2026-08-03
excluded packagepackage51143-54151143-541-93IInactivated by FDA2026-08-03
excluded packagepackage51143-54151143-541-96IInactivated by FDA2026-08-03
excluded packagepackage51143-54151143-541-97IInactivated by FDA2026-08-03

Observed NDC auxiliary status history#

Observed captured status history: Rows come only from successfully parsed FDA auxiliary ZIP captures. They show the state present in that artifact, not a continuous regulatory timeline. Absence before, after, or between captures is not proof of status, and a known non-data HTTP 403 capture is preserved in backfill provenance but cannot produce a status row.

Historic NDC status page 1 of 1 · 16 matching rows.

Browse every current auxiliary row. · Browse the complete NDC auxiliary source catalog.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2021-12-27 23:28 UTC · source 2021-12-27excluded productproduct51143-541IInactivated by FDAexcluded / ndc_excluded.zip8dfbde2a14a4…c9ff85d89658…
2021-12-27 23:28 UTC · source 2021-12-27excluded packagepackage51143-54151143-541-93IInactivated by FDAexcluded / ndc_excluded.zip8dfbde2a14a4…c9ff85d89658…
2021-12-27 23:28 UTC · source 2021-12-27excluded packagepackage51143-54151143-541-97IInactivated by FDAexcluded / ndc_excluded.zip8dfbde2a14a4…c9ff85d89658…
2021-12-27 23:28 UTC · source 2021-12-27excluded packagepackage51143-54151143-541-96IInactivated by FDAexcluded / ndc_excluded.zip8dfbde2a14a4…c9ff85d89658…
2020-12-18 03:04 UTC · source 2020-12-17excluded productproduct51143-541IInactivated by FDAexcluded / ndc_excluded.zipe2bbac7714bc…27bdfed8d636…
2020-12-18 03:04 UTC · source 2020-12-17excluded packagepackage51143-54151143-541-93IInactivated by FDAexcluded / ndc_excluded.zipe2bbac7714bc…27bdfed8d636…
2020-12-18 03:04 UTC · source 2020-12-17excluded packagepackage51143-54151143-541-97IInactivated by FDAexcluded / ndc_excluded.zipe2bbac7714bc…27bdfed8d636…
2020-12-18 03:04 UTC · source 2020-12-17excluded packagepackage51143-54151143-541-96IInactivated by FDAexcluded / ndc_excluded.zipe2bbac7714bc…27bdfed8d636…
2020-06-10 20:45 UTC · source 2020-06-10excluded productproduct51143-541IInactivated by FDAexcluded / ndc_excluded.zip9bebd1f3094a…5416666fcb17…
2020-06-10 20:45 UTC · source 2020-06-10excluded packagepackage51143-54151143-541-93IInactivated by FDAexcluded / ndc_excluded.zip9bebd1f3094a…5416666fcb17…
2020-06-10 20:45 UTC · source 2020-06-10excluded packagepackage51143-54151143-541-97IInactivated by FDAexcluded / ndc_excluded.zip9bebd1f3094a…5416666fcb17…
2020-06-10 20:45 UTC · source 2020-06-10excluded packagepackage51143-54151143-541-96IInactivated by FDAexcluded / ndc_excluded.zip9bebd1f3094a…5416666fcb17…
2019-12-08 06:16 UTC · source 2019-12-05excluded productproduct51143-541EExcluded after deficient or non-compliant submission was not correctedexcluded / ndc_excluded.zip110d247fa046…a55b01930146…
2019-12-08 06:16 UTC · source 2019-12-05excluded packagepackage51143-54151143-541-97EExcluded after deficient or non-compliant submission was not correctedexcluded / ndc_excluded.zip110d247fa046…a55b01930146…
2019-12-08 06:16 UTC · source 2019-12-05excluded packagepackage51143-54151143-541-93EExcluded after deficient or non-compliant submission was not correctedexcluded / ndc_excluded.zip110d247fa046…a55b01930146…
2019-12-08 06:16 UTC · source 2019-12-05excluded packagepackage51143-54151143-541-96EExcluded after deficient or non-compliant submission was not correctedexcluded / ndc_excluded.zip110d247fa046…a55b01930146…

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51143-541-932020-01-31C16284748780-19d75b9d0-23a4-f424-e053-dadaa90a57ceDrug Facts
51143-541-962020-01-31C16284748780-19d75b9d0-23a4-f424-e053-dadaa90a57ceDrug Facts
51143-541-972020-01-31C16284748780-19d75b9d0-23a4-f424-e053-dadaa90a57ceDrug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
TRICLOSANACTIVE INGREDIENT4NM5039Y5XANTIBACTERIAL LIQUID HAND (TRICLOSAN) LIQUID [ONPOINT, INC]1
TRICLOSANACTIVE MOIETY4NM5039Y5XANTIBACTERIAL LIQUID HAND (TRICLOSAN) LIQUID [ONPOINT, INC]1
COCAMIDOPROPYL BETAINEINACTIVE INGREDIENT5OCF3O11KXANTIBACTERIAL LIQUID HAND (TRICLOSAN) LIQUID [ONPOINT, INC]1
DMDM HYDANTOININACTIVE INGREDIENTBYR0546TOWANTIBACTERIAL LIQUID HAND (TRICLOSAN) LIQUID [ONPOINT, INC]1
PEG-120 METHYL GLUCOSE DIOLEATEINACTIVE INGREDIENTYM0K64F20VANTIBACTERIAL LIQUID HAND (TRICLOSAN) LIQUID [ONPOINT, INC]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XANTIBACTERIAL LIQUID HAND (TRICLOSAN) LIQUID [ONPOINT, INC]1
SODIUM LAURETH SULFATEINACTIVE INGREDIENTBPV390UAP0ANTIBACTERIAL LIQUID HAND (TRICLOSAN) LIQUID [ONPOINT, INC]1
SODIUM LAURYL SULFATEINACTIVE INGREDIENT368GB5141JANTIBACTERIAL LIQUID HAND (TRICLOSAN) LIQUID [ONPOINT, INC]1