SFT1 Sanitizing Wipes

Manufacturer
ORR Safety
Effective date
2023-10-26
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:57:49

Label at a glance#

ProductSFT1 Sanitizing Wipes
Active ingredientALCOHOL
Label structure7 sections

Label contents#

Full prescribing information#

Active ingredient [s]

OTC - ACTIVE INGREDIENT SECTION

75% Ethyl Alcohol 

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use[s]

INDICATIONS & USAGE SECTION

  • Helps reduce bacteria on the kin
  • Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.Flammable. keep away from fire or flame

Do not use in eyes.

OTC - DO NOT USE SECTION

If contact occurs, flush thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop and persist for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Direction

DOSAGE & ADMINISTRATION SECTION

  • Use one wipe per object to avoid cross contamination
  • Allow to dry without wiping
  • Discard wipe in trash receptacle after use
  • Do not flush
  • For dispending, peel back front label at tab
  • Remove pouch by pressing label firmly back into place 

Other information

SPL UNCLASSIFIED SECTION

  • Store below 104 °F (40 °C)
  • May discolor certain fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 wipes50 wipes

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79401-002-50SFT1 Sanitizing Wipes50 in 1 POUCHCLOTH503
79401-002-50SFT1 Sanitizing Wipes5.4 mL in 1 PATCHCLOTH5.43

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79401-002SFT1 SANITIZING WIPES (ALCOHOL) CLOTH [ORR SAFETY]3Current NDC, Legacy NDC, 2 package rows20231026_b787fa1d-1e15-245b-e053-2a95a90a00a1.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
79401-00279401-002-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
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
SFT1 Sanitizing WipesALCOHOLORR Safetyb787fa1d-1e15-245b-e053-2a95a90a00a12023-10-26WarningsExact identifier
ndc (package): 79401-002-50
ndc (product): 79401-002
ndc11 (package): 79401000250
spl id: 0898be5e-2a1f-7c7f-e063-6294a90ac297
spl set id: b787fa1d-1e15-245b-e053-2a95a90a00a1

Reported adverse events (FAERS/openFDA)#

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