Travel Wipes Moisturizer and fragrance

Manufacturer
SINGULAR ENTERPRISES LLC
Effective date
2025-06-06
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:02:29

Label at a glance#

ProductTravel Wipes Moisturizer and fragrance
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Hand sanitizing to decrease bacteria on skin. Recommended for repeated use.

Dosage and administration

Tear open package and unfold wipe.  Thoroughly wipe hands fingers and wrists.  Be sure to use entire wipe for approximately 20 seconds.  No rinsing or toweling is required.  Discard after single use. Do not flush.

Label contents#

Full prescribing information#

Active Ingredient (s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand sanitizing to decrease bacteria on skin. Recommended for repeated use.

Warnings

WARNINGS SECTION

  • For external use only. 
  • Flammable, keep away from fire or flame. 
  • Do not use this product in or near eyes. If contact occurs, rinse thoroughly with water. 
  • Keep out of reach of children unless under adult supervision. 
  • Discontinue use if skin irritation and redness develop. 
  • If condition persists for more than 72 hours consult a physician.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Tear open package and unfold wipe. 
  • Thoroughly wipe hands fingers and wrists. 
  • Be sure to use entire wipe for approximately 20 seconds. 
  • No rinsing or toweling is required. 
  • Discard after single use. Do not flush.

Inactive Ingredients.

INACTIVE INGREDIENT SECTION

Purified Water, glycerine, hydrogen peroxide, fragrance

Other information (if applicable)

OTHER SAFETY INFORMATION

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

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1489307ethanol 70 % Medicated PadPSN3
1489307ethanol 0.7 ML/ML Medicated PadSCD3
1489307ethanol 70 % Medicated PadSY3
1489307ethanol 70 % Medicated WipesSY3
1489307ethyl alcohol 70 % ClothSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81428-074-01Travel Wipes Moisturizer and fragrance15 in 1 BOXCLOTH153
81428-074-01Travel Wipes Moisturizer and fragrance4 mL in 1 POUCHCLOTH43
81428-074-02Travel Wipes Moisturizer and fragrance30 in 1 BOXCLOTH303
81428-074-02Travel Wipes Moisturizer and fragrance4 mL in 1 POUCHCLOTH43
81428-074-03Travel Wipes Moisturizer and fragrance50 in 1 BOXCLOTH503
81428-074-03Travel Wipes Moisturizer and fragrance4 mL in 1 POUCHCLOTH43
81428-074-04Travel Wipes Moisturizer and fragrance100 in 1 BOXCLOTH1003
81428-074-04Travel Wipes Moisturizer and fragrance4 mL in 1 POUCHCLOTH43

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81428-07481428-074-01, 81428-074-02, 81428-074-03, 81428-074-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
Travel Wipes Moisturizer and fragranceALCOHOLSINGULAR ENTERPRISES LLC46024d13-84dd-47a9-af76-d2feba62448c2025-06-06WarningsExact identifier
ndc (package): 81428-074-04
ndc (package): 81428-074-03
ndc (package): 81428-074-02
ndc (package): 81428-074-01
ndc (product): 81428-074
ndc11 (package): 81428007404
ndc11 (package): 81428007401
ndc11 (package): 81428007403
ndc11 (package): 81428007402
spl id: 36e6baf2-cb09-9de0-e063-6394a90af8af
spl set id: 46024d13-84dd-47a9-af76-d2feba62448c

Reported adverse events (FAERS/openFDA)#

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