FDA.reportPublic FDA data

Cskin Hand Sanitizing Wipe

Manufacturer
Medics Medical Products LLC
Effective date
2020-12-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:35:42

Label at a glance#

ProductCskin Hand Sanitizing Wipe
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Tear open packet. Unfold and apply wipe thoroughly onto hands. Discard after single use. Discard after single use. No rinsing required.Dispose of used wipes in the trash. Do not flush.

Storage and handling

Store between 15-30C (59-86F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire, flame, or sources of ignition.

Do not use

OTC - DO NOT USE SECTION

in or contact with eyes.

OTC - WHEN USING SECTION





Keep out of reach of children, unless under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Discontinue use if irritation and redness develops. If condition persists more than 72 hours, cosult a doctor.

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

  • Tear open packet. Unfold and apply wipe thoroughly onto hands.
  • Discard after single use. Discard after single use. No rinsing required.Dispose of used wipes in the trash.
  • Do not flush.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

fragrance, glycerin, purified water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Info panelInfo panelcskincskinNDC: 80461-001-01

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80461-001-012022-01-28C16284748780-1d6a99b39-ce25-a426-e053-dadaa90af4c2Cskin Instant Hand Sanitizing Wipe

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80461-001-01Cskin Hand Sanitizing Wipe1 mL in 1 PACKETSOLUTION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80461-001CSKIN HAND SANITIZING WIPE (ETHYL ALCOHOL) SOLUTION [MEDICS MEDICAL PRODUCTS LLC]1Legacy NDC, 1 package rows20201223_b69d1509-dd84-9c19-e053-2995a90a8a56.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80461-00180461-001-01

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
b69d160a-291d-897b-e053-2a95a90ae31db69d1509-dd84-9c19-e053-2995a90a8a562020-12-21WarningsExact identifier
spl id: b69d160a-291d-897b-e053-2a95a90ae31d
spl set id: b69d1509-dd84-9c19-e053-2995a90a8a56

Reported adverse events (FAERS/openFDA)#

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