Dr. Oracle OH MY CLEAN Hand Sanitizer

Manufacturer
Oracle Cosmetic Co., Ltd. | SISKINKOREA CO.,LTD.
Effective date
2020-07-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:20:43

Label at a glance#

ProductDr. Oracle OH MY CLEAN Hand Sanitizer
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

03 500 7003 500 70

WARNINGS SECTION

OTC - ACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

DOSAGE & ADMINISTRATION SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - DO NOT USE SECTION

OTC - PURPOSE SECTION

OTC - STOP USE SECTION

INDICATIONS & USAGE SECTION

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71883-003-012023-05-26C16284748780-1f386c649-bce6-0266-e053-dadaa90a7c1a71883-003_Dr. Oracle OH MY CLEAN Hand Sanitizer
71883-003-012023-01-30C16284748780-1f386c649-bce6-0266-e053-dadaa90a7c1a71883-003_Dr. Oracle OH MY CLEAN Hand Sanitizer

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71883-00371883-003-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
fc9db41a-9c5c-9ab6-e053-6394a90abe072df801d7-08ed-426e-be88-94e49a0104392023-05-26Exact identifier
spl set id: 2df801d7-08ed-426e-be88-94e49a010439

Reported adverse events (FAERS/openFDA)#

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