FDA.reportPublic FDA data

ANTI BYE SANITIZER WIPES

Manufacturer
Perfumeholic Inc
Effective date
2020-09-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:30:21

Label at a glance#

ProductANTI BYE SANITIZER WIPES
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ANTI BYE HAND SANITIZER WIPESANTI BYE HAND SANITIZER WIPES

OTC - ACTIVE INGREDIENT SECTION

DOSAGE & ADMINISTRATION SECTION

OTC - PURPOSE SECTION

INDICATIONS & USAGE SECTION

INACTIVE INGREDIENT SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - WHEN USING SECTION

INSTRUCTIONS FOR USE SECTION

WARNINGS SECTION

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75773-375-502022-07-29C16284748780-1e4f33bdf-a3f1-d8a0-e053-dadaa90a6e4ePerfumeholic Inc | ANTI BYE SANITIZER WIPES | 75773-375-50 | 50 WIPES

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75773-375-50ANTI BYE SANITIZER WIPES50 in 1 CANISTERCLOTH502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75773-375ANTI BYE SANITIZER WIPES (ALCOHOL) CLOTH [PERFUMEHOLIC INC]2Legacy NDC, 1 package rows20200928_acd177ba-7588-5e11-e053-2995a90a046b.zip

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
75773-37575773-375-50

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
BUTYLENE GLYCOL3XUS85K0RAIACT
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
CHAMOMILEFGL3685T2XIACT
PEG-60 HYDROGENATED CASTOR OIL02NG325BQGIACT
LAVENDER OILZBP1YXW0H8IACT
SODIUM BENZOATEOJ245FE5EUIACT
ALCOHOL3K9958V90MACTIB

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
b0597ddf-c113-20e7-e053-2a95a90a641facd177ba-7588-5e11-e053-2995a90a046b2020-09-28Exact identifier
spl id: b0597ddf-c113-20e7-e053-2a95a90a641f
spl set id: acd177ba-7588-5e11-e053-2995a90a046b

Reported adverse events (FAERS/openFDA)#

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