FDA.reportPublic FDA data

Wet Wipe 36 Pack

Manufacturer
Sea to Summit Pty Ltd
Effective date
2021-11-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:44:55

Label at a glance#

ProductWet Wipe 12 Pack
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

SaniWipes Drug FactsSaniWipes Drug Facts

OTC - PURPOSE SECTION

purposepurpose

INDICATIONS & USAGE SECTION

usageusage

WARNINGS SECTION

warningwarning

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

childrenchildren

DOSAGE & ADMINISTRATION SECTION

dosagedosage

INACTIVE INGREDIENT SECTION

inactiveinactive

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SaniWipes 12SaniWipes 12SaniWipes 36SaniWipes 36

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN3
1307051ethanol 0.75 ML/ML Medicated PadSCD3
1307051ethanol 75 % Hand Sanitizer WipesSY3
1307051ethyl alcohol 75 % Topical ClothSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79238-1120-12023-01-30C16284748780-1f386c649-feff-0266-e053-dadaa90a7c1aWet Wipe 75% Alcohol; 12 Count, 36 Count
79238-1121-12023-01-30C16284748780-1f386c649-feff-0266-e053-dadaa90a7c1aWet Wipe 75% Alcohol; 12 Count, 36 Count

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79238-1120-1Wet Wipe 12 Pack75 mL in 1 BAGSWAB753
79238-1121-1Wet Wipe 36 Pack220 mL in 1 BAGSWAB2203

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79238-1120WET WIPE 12 PACK (ALCOHOL) SWAB WET WIPE 36 PACK (ALCOHOL) SWAB [SEA TO SUMMIT PTY LTD]3Legacy NDC, 1 package rows20211116_ad10ad36-9229-faef-e053-2995a90acd5b.zip
79238-1121WET WIPE 12 PACK (ALCOHOL) SWAB WET WIPE 36 PACK (ALCOHOL) SWAB [SEA TO SUMMIT PTY LTD]3Legacy NDC, 1 package rows20211116_ad10ad36-9229-faef-e053-2995a90acd5b.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
79238-112079238-1120-1
79238-112179238-1121-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
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
d0cdb64d-fb4f-be9b-e053-2995a90aed7fad10ad36-9229-faef-e053-2995a90acd5b2021-11-15WarningsExact identifier
spl id: d0cdb64d-fb4f-be9b-e053-2995a90aed7f
spl set id: ad10ad36-9229-faef-e053-2995a90acd5b

Reported adverse events (FAERS/openFDA)#

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