FDA.reportPublic FDA data

ANTI BYE DISINFECTING WIPES

Manufacturer
Perfumeholic Inc
Effective date
2020-12-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:34:34

Label at a glance#

ProductANTI BYE DISINFECTING WIPES
Active ingredientBENZALKONIUM CHLORIDE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ANTI BYE DISINFECTING WIPESANTI BYE DISINFECTING 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
75773-013-802022-07-29C16284748780-1e4f33bdf-9de2-d8a0-e053-dadaa90a6e4ePerfumeholic Inc | ANTI BYE DISINFECTING WIPES | 75773-013-80 | 80 WIPES

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75773-013-80ANTI BYE DISINFECTING WIPES80 in 1 PACKETCLOTH801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75773-013ANTI BYE DISINFECTING WIPES (BENZALKONIUM CHLORIDE) CLOTH [PERFUMEHOLIC INC]1Legacy NDC, 1 package rows20201203_b5887bfa-1f7c-e883-e053-2995a90ad473.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75773-01375773-013-80

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
PEG-60 HYDROGENATED CASTOR OIL02NG325BQGIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
SODIUM BENZOATEOJ245FE5EUIACT
LAVENDER OILZBP1YXW0H8IACT

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
b58881d0-93f4-ddb4-e053-2995a90af986b5887bfa-1f7c-e883-e053-2995a90ad4732020-12-02Exact identifier
spl id: b58881d0-93f4-ddb4-e053-2995a90af986
spl set id: b5887bfa-1f7c-e883-e053-2995a90ad473

Reported adverse events (FAERS/openFDA)#

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