FDA.reportPublic FDA data

LATHER - LAVENDER HAND SANITIZING WIPES

Manufacturer
Lather, Inc.
Effective date
2023-10-03
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-01 21:25:12

Label at a glance#

ProductLATHER - LAVENDER HAND SANITIZING WIPES WITH MOISTURIZING ALOE
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin when water and soap are not available. Recommended for repeated use.

Dosage and administration

Remove wipe Wet hands thoroughly with wipe and allow hands to dry without wiping.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 65% v/v

PURPOSE

OTC - PURPOSE SECTION

ANTIMICROBIAL

USES

INDICATIONS & USAGE SECTION

  • For hand sanitizing to decrease bacteria on the skin when water and soap are not available.
  • Recommended for repeated use.

WARNINGS

WARNINGS SECTION

For external use only. Flammable: keep away from fire or flame. When using this product do not use in or near eyes. If contact occurs, flush thoroughly with water. Stop use and contact a doctor if irritation or redness persists for more than 72hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • Remove wipe
  • Wet hands thoroughly with wipe and allow hands to dry without wiping.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, glycerin, lavandula angustifolia (lavender) oil, organic aloe barbadensis leaf extract, organic althaea officinalis (marshmallow) root extract, organic avena sativa (oat) kernel extract, organic camellia sinensis (white tea) leaf extract, organic chamomilla recutita (matricaria) flower extract, organic cucumis sativus (cucumber) fruit extract.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_HandSanitizingWipes-10pack_FDA01b LBL_HandSanitizingWipes-10pack_FDA

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77394-10377394-103-01, 77394-103-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
LAVENDER OILZBP1YXW0H8IACT
ALOE VERA LEAFZY81Z83H0XIACT
ALTHAEA OFFICINALIS ROOTTRW2FUF47HIACT
OATZ6J799EAJKIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
MATRICARIA CHAMOMILLA FLOWERING TOP3VNC7T6Z02IACT
CUCUMBERYY7C30VXJTIACT
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
2c7d5d72-fdcc-15ee-e063-6394a90a7da1eb17d287-385f-4a2d-99f8-8ecbb350acad2025-01-24WarningsExact identifier
spl set id: eb17d287-385f-4a2d-99f8-8ecbb350acad

Reported adverse events (FAERS/openFDA)#

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