FDA.reportPublic FDA data

SurviveX BZK Antiseptic Towelettes

Manufacturer
Taizhou Kangping Medical Science And Technology Co., Ltd.
Effective date
2024-10-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:23:21

Label at a glance#

ProductSurviveX BZK Antiseptic Towelettes
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

DOSAGEDOSAGE

WARNINGS SECTION

warningwarning

INACTIVE INGREDIENT SECTION

inactive ingredientinactive ingredient

INDICATIONS & USAGE SECTION

IndicationIndication

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

OTC - PURPOSE SECTION

purposepurpose

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PACKAGE LABELPACKAGE LABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN1
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD1
1038558benzalkonium chloride 0.13 % Topical ClothSY1
1038558benzalkonium chloride 0.13 % Topical SwabSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY1
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71310-115-01SurviveX BZK Antiseptic Towelettes1.6 g in 1 POUCHLIQUID1.61

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71310-115SURVIVEX BZK ANTISEPTIC TOWELETTES (BENZALKONIUM CHLORIDE) LIQUID [TAIZHOU KANGPING MEDICAL SCIENCE AND TECHNOLOGY CO., LTD.]11 package rows20241010_23f4fbe6-1e66-0be9-e063-6394a90abb13.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71310-11571310-115-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT

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
23f4fbe6-1e67-0be9-e063-6394a90abb1323f4fbe6-1e66-0be9-e063-6394a90abb132024-10-08WarningsExact identifier
spl id: 23f4fbe6-1e67-0be9-e063-6394a90abb13
spl set id: 23f4fbe6-1e66-0be9-e063-6394a90abb13

Reported adverse events (FAERS/openFDA)#

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