FDA.reportPublic FDA data

SPECTRUM HAND SANITIZER WIPES

Manufacturer
Medline Industries, Inc.
Effective date
2023-10-27
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-05-31 23:58:21

Label at a glance#

ProductSPECTRUM HAND SANITIZER WIPES
Active ingredientALCOHOL
Label structure15 sections

Indications and uses

to decrease bacteria on the skin that could cause disease

Dosage and administration

wet hands thoroughly with product and allow to dry not recommended for infants

Storage and handling

do not store above 105ºF may discolor some fabrics harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin that could cause disease

Warnings

WARNINGS SECTION

For external use only: hands

Flammable. Keep away from fire and flame.

OTC - WHEN USING SECTION

When using this product

keep out of eyes. In case of contact with eyes, flush thoroughly with water.
avoid contact with broken skin
do not inhale or ingest

OTC - STOP USE SECTION

Stop use and ask a doctor if

irritation or redness develops
condition persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product and allow to dry

not recommended for infants

other information

STORAGE AND HANDLING SECTION

do not store above 105ºF
may discolor some fabrics
harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe barbadensis leaf juice, glycerin, isopropanol, propanediol, tocopheryl acetate, water

Uses

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin that could cause disease

recommended for repeated use

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product and allow to dry without wiping
not recommended for infants

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

20 WIPES, NDC: 53329-998-01

20 pcs label20 pcs label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 WIPES, NDC: 53329-998-02

50 pcs label50 pcs label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

160 WIPES, NDC: 53329-998-03

160 pcs label160 pcs label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1489307ethanol 70 % Medicated PadPSN8
1489307ethanol 0.7 ML/ML Medicated PadSCD8
1489307ethanol 70 % Medicated PadSY8
1489307ethanol 70 % Medicated WipesSY8
1489307ethyl alcohol 70 % ClothSY8

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53329-998-012026-01-29C16284748780-149896155-d668-586f-e063-e6dba90add90SPECTRUM HAND SANITIZER WIPES
53329-998-022026-01-29C16284748780-149896155-d668-586f-e063-e6dba90add90SPECTRUM HAND SANITIZER WIPES
53329-998-032026-01-29C16284748780-149896155-d668-586f-e063-e6dba90add90SPECTRUM HAND SANITIZER WIPES

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53329-998-01SPECTRUM HAND SANITIZER WIPES20 in 1 PACKAGECLOTH208
53329-998-01SPECTRUM HAND SANITIZER WIPES1.32 mL in 1 APPLICATORCLOTH1.328
53329-998-02SPECTRUM HAND SANITIZER WIPES2.55 mL in 1 APPLICATORCLOTH2.558
53329-998-02SPECTRUM HAND SANITIZER WIPES50 in 1 CANISTERCLOTH508
53329-998-03SPECTRUM HAND SANITIZER WIPES160 in 1 CANISTERCLOTH1608
53329-998-03SPECTRUM HAND SANITIZER WIPES1.2 mL in 1 APPLICATORCLOTH1.28

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53329-998SPECTRUM HAND SANITIZER WIPES (ALCOHOL WIPES) CLOTH [MEDLINE INDUSTRIES, INC.]8Legacy NDC, 6 package rows20231030_c1b93f28-1ae5-9e63-e053-2a95a90af8a4.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53329-99853329-998-01, 53329-998-02, 53329-998-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPANEDIOL5965N8W85TIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ISOPROPYL ALCOHOLND2M416302IACT
ALCOHOL3K9958V90MACTIB
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
08ad6da5-252b-78b1-e063-6294a90a9446c1b93f28-1ae5-9e63-e053-2a95a90af8a42023-10-27WarningsExact identifier
spl id: 08ad6da5-252b-78b1-e063-6294a90a9446
spl set id: c1b93f28-1ae5-9e63-e053-2a95a90af8a4