FDA.reportPublic FDA data

UNSCENTED HAND SANITIZER

Manufacturer
Strategic Sourcing Services LLC
Effective date
2021-08-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:39:11

Label at a glance#

ProductUNSCENTED HAND SANITIZER SUNMARK
Active ingredientALCOHOL
Label structure13 sections

Indications and uses

hand sanitizer to help reduce bacteria on the skin that could cause disease.

Dosage and administration

spray enough product in palm to thoroughly cover your hands rub hands together briskly until dry children under 6 years of age should be supervised when using this product.

Storage and handling

may discolor or damage some fabrics/materials or surfaces. Avoid freezing and excessive heat above 40ºC (104ºF).

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • hand sanitizer to help reduce bacteria on the skin that could cause disease.

Warnings

WARNINGS SECTION

For external use only. .

Flammable.

WARNINGS AND PRECAUTIONS SECTION

Keep away from heat or flame. Do not use while smoking

Do not use

OTC - DO NOT USE SECTION

  • on children less than 2 months of age
  • on open skin wounds

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water to remove.
  • do not puncture or incinerate. Contents under pressure. Do not store at temperatufes above 120ºF.

Stop use and ask a doctor if

OTC - STOP USE SECTION

rash or irritation occurs. These may be signs of a serious condition.

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

  • spray enough product in palm to thoroughly cover your hands
  • rub hands together briskly until dry
  • children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

  • may discolor or damage some fabrics/materials or surfaces.
  • Avoid freezing and excessive heat above 40ºC (104ºF).

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, aloe barbadensis leaf juice, tocopheryl acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MK95385DMK95385D

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49348-28749348-287-37

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
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
f160e707-3209-22f9-e053-2995a90ac056aa53aa1f-53b1-8ded-e053-2a95a90afde02023-01-03WarningsExact identifier
spl set id: aa53aa1f-53b1-8ded-e053-2a95a90afde0

Reported adverse events (FAERS/openFDA)#

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