LATHER- HAND SANITIZER WITH MOISTURIZING ALOE

Manufacturer
Lather, Inc.
Effective date
2021-12-01
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:25:13

Label at a glance#

ProductLATHER- HAND SANITIZER WITH MOISTURIZING ALOE 70 PERCENT
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

HAND SANITIZER TO HELP REDUCE BACTERIA ON THE SKIN. RECOMMENDED FOR REPEATED USE.

Dosage and administration

Dispense an adequate amount in your palm to cover all surfaces of hands completely. Rub hands together until dry. Does not require rinsing.

Storage and handling

do not store above 100°F may discolor some fabrics

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 70%

PURPOSE

OTC - PURPOSE SECTION

ANTIMICROBIAL

USES

INDICATIONS & USAGE SECTION

  • HAND SANITIZER TO HELP REDUCE BACTERIA ON THE SKIN.
  • RECOMMENDED FOR REPEATED USE.

WARNINGS

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

Do not use in or near eyes. In case of eye contact, flush thoroughly with water and seek medical attention.

Stop use and ask a doctor if irritation and redness develop and persists for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • Dispense an adequate amount in your palm to cover all surfaces of hands completely.
  • Rub hands together until dry.
  • Does not require rinsing.

OTHER INFORMATION:

STORAGE AND HANDLING SECTION

  • do not store above 100°F
  • may discolor some fabrics

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol, Orange Oil, ACrylates/C10-30 Alkyl Acrylate Crosspolymer, Glycerin, Aloe Barbadensis Leaf Juice, Panthenol, Aminomethyl Propanol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_HandSanitizer_2oz_Label_R101b LBL_HandSanitizer_2oz_Label_R1

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77394-10277394-102-11, 77394-102-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

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
06d49422-3f97-f930-e063-6294a90a27eb89cc0ceb-5dbf-4b38-9d26-aabc0e1f49e82023-10-03WarningsExact identifier
spl set id: 89cc0ceb-5dbf-4b38-9d26-aabc0e1f49e8

Reported adverse events (FAERS/openFDA)#

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