FDA.reportPublic FDA data

Singular Wipes

Manufacturer
SINGULAR ENTERPRISES LLC
Effective date
2025-06-06
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:02:26

Label at a glance#

ProductSingular Wipes
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 (Aqua), 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 PadPSN9
1489307ethanol 0.7 ML/ML Medicated PadSCD9
1489307ethanol 70 % Medicated PadSY9
1489307ethanol 70 % Medicated WipesSY9
1489307ethyl alcohol 70 % ClothSY9

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81428-070-042024-08-02C16284748780-11030e365-2384-111a-e063-dadaa90a10e203957345-ccd0-4def-b528-7733e6a24cbb
81428-070-052024-08-02C16284748780-11030e365-2384-111a-e063-dadaa90a10e203957345-ccd0-4def-b528-7733e6a24cbb
81428-070-062024-08-02C16284748780-11030e365-2384-111a-e063-dadaa90a10e203957345-ccd0-4def-b528-7733e6a24cbb
81428-070-072024-08-02C16284748780-11030e365-2384-111a-e063-dadaa90a10e203957345-ccd0-4def-b528-7733e6a24cbb
81428-070-082024-08-02C16284748780-11030e365-2384-111a-e063-dadaa90a10e203957345-ccd0-4def-b528-7733e6a24cbb
81428-070-042024-07-30C16284748780-11030e365-2384-111a-e063-dadaa90a10e203957345-ccd0-4def-b528-7733e6a24cbb
81428-070-052024-07-30C16284748780-11030e365-2384-111a-e063-dadaa90a10e203957345-ccd0-4def-b528-7733e6a24cbb
81428-070-062024-07-30C16284748780-11030e365-2384-111a-e063-dadaa90a10e203957345-ccd0-4def-b528-7733e6a24cbb
81428-070-072024-07-30C16284748780-11030e365-2384-111a-e063-dadaa90a10e203957345-ccd0-4def-b528-7733e6a24cbb
81428-070-082024-07-30C16284748780-11030e365-2384-111a-e063-dadaa90a10e203957345-ccd0-4def-b528-7733e6a24cbb
81428-070-042024-01-30C16284748780-11030e365-2384-111a-e063-dadaa90a10e203957345-ccd0-4def-b528-7733e6a24cbb
81428-070-052024-01-30C16284748780-11030e365-2384-111a-e063-dadaa90a10e203957345-ccd0-4def-b528-7733e6a24cbb
81428-070-062024-01-30C16284748780-11030e365-2384-111a-e063-dadaa90a10e203957345-ccd0-4def-b528-7733e6a24cbb
81428-070-072024-01-30C16284748780-11030e365-2384-111a-e063-dadaa90a10e203957345-ccd0-4def-b528-7733e6a24cbb
81428-070-082024-01-30C16284748780-11030e365-2384-111a-e063-dadaa90a10e203957345-ccd0-4def-b528-7733e6a24cbb

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81428-070-04Singular Wipes4 mL in 1 POUCHCLOTH49
81428-070-05Singular Wipes24 in 1 BOXCLOTH249
81428-070-05Singular Wipes4 mL in 1 POUCHCLOTH49
81428-070-06Singular Wipes24 in 1 BAGCLOTH249
81428-070-06Singular Wipes4 mL in 1 POUCHCLOTH49
81428-070-07Singular Wipes4 mL in 1 POUCHCLOTH49
81428-070-07Singular Wipes100 in 1 BOXCLOTH1009
81428-070-08Singular Wipes15 in 1 BOXCLOTH159
81428-070-08Singular Wipes4 mL in 1 POUCHCLOTH49

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
81428-07081428-070-04, 81428-070-05, 81428-070-06, 81428-070-07, 81428-070-08

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
LEMON TERPENES5DHA4TVW63IACT
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
Singular WipesALCOHOLSINGULAR ENTERPRISES LLC03957345-ccd0-4def-b528-7733e6a24cbb2025-06-06WarningsExact identifier
ndc (package): 81428-070-04
ndc (package): 81428-070-08
ndc (package): 81428-070-07
ndc (package): 81428-070-06
ndc (package): 81428-070-05
ndc (product): 81428-070
ndc11 (package): 81428007004
ndc11 (package): 81428007008
ndc11 (package): 81428007006
ndc11 (package): 81428007005
ndc11 (package): 81428007007
spl id: 36e6b2ce-d188-9c90-e063-6394a90a4566
spl set id: 03957345-ccd0-4def-b528-7733e6a24cbb

Reported adverse events (FAERS/openFDA)#

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