Elyptol Hand Sanitizer Wipe

Manufacturer
Elyptol Inc.
Effective date
2021-12-22
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-05-31 23:45:52

Label at a glance#

ProductElyptol Hand Sanitizer Wipe
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

To decrease bacteria on skin. Recommended for repeated use.

Dosage and administration

Tear open sachet. Unfold towelette and wipe hands thoroughly. No need to rinse.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua (Purified Water), Eucalyptol, Glyercin

Purpose

OTC - PURPOSE SECTION

Skin antiseptic

Warnings

WARNINGS SECTION

For external use only.

Flammable.. Keep away from sources of fire or flame.

When using this product

Keep away from eyes. In case of eye contact, rinse eyes with water.

Stop use and ask a doctor if

redness or irritation develops and issues persist, seek medical attention.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Tear open sachet.
  • Unfold towelette and wipe hands thoroughly.
  • No need to rinse.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Other Information

OTHER SAFETY INFORMATION

  • Store below 86F / 30C
  • Keep out of direct sunlight
  • May discolor some fabrics
  • Lot No. and Expiration Date can be found on packet

Uses

INDICATIONS & USAGE SECTION

  • To decrease bacteria on skin.
  • Recommended for repeated use.

OTC - QUESTIONS SECTION

Questions? (888) 424-9874

SPL UNCLASSIFIED SECTION

  • 100% biobased ingredients
  • Kills 99.9% of Most Common Germs
  • Pure Eucalyptus Oil • Gentle on Your Skin
  • Dermatologically Tested • Not tested on Animals

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1489307ethanol 70 % Medicated PadPSN7
1489307ethanol 0.7 ML/ML Medicated PadSCD7
1489307ethanol 70 % Medicated PadSY7
1489307ethanol 70 % Medicated WipesSY7
1489307ethyl alcohol 70 % ClothSY7

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69343-322-01Elyptol Hand Sanitizer Wipe1 in 1 POUCHCLOTH17
69343-322-06Elyptol Hand Sanitizer Wipe6 in 1 CARTONCLOTH67
69343-322-10Elyptol Hand Sanitizer Wipe10 in 1 PACKETCLOTH107
69343-322-24Elyptol Hand Sanitizer Wipe24 in 1 CARTONCLOTH247
69343-322-60Elyptol Hand Sanitizer Wipe6 in 1 CARTONCLOTH67
69343-322-60Elyptol Hand Sanitizer Wipe1 in 1 CANISTERCLOTH17

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69343-322ELYPTOL HAND SANITIZER WIPE (ETHANOL) CLOTH [ELYPTOL INC.]7Legacy NDC, 6 package rows20211223_41851cf8-cf6d-70c1-e054-00144ff88e88.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
69343-32269343-322-01, 69343-322-24, 69343-322-10, 69343-322-06, 69343-322-60

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
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
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
d881d2d1-55bf-41b3-be62-371ce5f4c00841851cf8-cf6d-70c1-e054-00144ff88e882021-12-22WarningsExact identifier
spl id: d881d2d1-55bf-41b3-be62-371ce5f4c008
spl set id: 41851cf8-cf6d-70c1-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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