HAND SANITIZER

Manufacturer
PRESTIGE COSMETICS, INC.
Effective date
2021-11-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:29:44

Label at a glance#

ProductHAND SANITIZER WITH ALOE
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

HAND SANITIZER TO HELP REDUCE BACTERIA AND GERMS ON THE SKIN.

Dosage and administration

APPLY TO CLEAN, DRY HANDS AND ALLOW PRODUCT TO DRY WITHOUT WIPING FOR CHILDREN UNDER 6, USE ONLY UNDER ADULT SUPERVISION NOT RECOMMENDED FOR INFANTS

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 AND GERMS ON THE SKIN.

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY.

FLAMMABLE: KEEP AWAY FROM EXCESSIVE HEAT OR OPEN FLAME.

WHEN USING THIS PRODUCT USE ONLY AS DIRECTED

  • AVOID CONTACT WITH EYES, MOUTH AND MUCOUS MEMBRANES. IN CASE OF CONTACT, FLUSH THOROUGHLY WITH WATER.
  • AVOID CONTACT WITH BROKEN, WOUNDED OR IRRITATED SKIN.
  • DO NOT INHALE OR INGEST.
  • STORE IN A COOL, DRY PLACE AND DO NOT LEAVE IN DIRECT SUNLIGHT.
  • DO NOT USE ON SKIN AFTER EXPIRATION DATE.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - ASK DOCTOR SECTION

ASK A DOCTOR OR PHARMACIST IF YOU ARE CURRENTLY UNDER THE CARE OF A PHYSICIAN.

OTC - STOP USE SECTION

DISCONTINUE USE AND CONSULT A PHYSICIAN IF ANY SIGNS OF RASH OR IRRITATION APPEAR

  • ACCIDENTALLY INGESTED (OR CONTACT POISON CONTROL IMMEDIATELY)

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

APPLY TO CLEAN, DRY HANDS AND ALLOW PRODUCT TO DRY WITHOUT WIPING

  • FOR CHILDREN UNDER 6, USE ONLY UNDER ADULT SUPERVISION
  • NOT RECOMMENDED FOR INFANTS

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

PURIFIED WATER, GLYCERIN, ALOE BARBADENSIS, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, ISOPROPYL MYRISTATE, TOCOPHERYL ACETATE, CAPRYLYL GLYCOL, FRAGRANCE, FDC BLUE #1, YELLOW #5.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_EF Hand Santizer_4oz01b LBL_EF Hand Santizer_4oz

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
62279-10162279-101-11, 62279-101-12, 62279-101-13, 62279-101-14

Ingredients#

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

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

Source Document#

Source XML · Source PDF

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
e81ef3e7-1255-1c1f-e053-2995a90a0b1766bcbab7-0bd1-4046-aaae-dade585beb3e2022-09-07WarningsExact identifier
spl set id: 66bcbab7-0bd1-4046-aaae-dade585beb3e

Reported adverse events (FAERS/openFDA)#

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