Hand Sanitizer 80 Alcohol

Manufacturer
Servi Quim de Monterrey, S.A. de C.V.
Effective date
2020-07-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:20:50

Label at a glance#

ProductHand Sanitizer 80 Alcohol
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Place enough product on hands to coverall surfaces. Rub hands together until dry. Super vise children under 6 years of age when using this product to avoids wallowing.

Label contents#

Full prescribing information#

Active ingredient[s]

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use[s]

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use 

OTC - DO NOT USE SECTION

  • in 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.

Stop use and ask a doctor 

OTC - STOP USE SECTION

if irritation or rash occurs. These may be signs or 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

  • Place enough product on hands to coverall surfaces. Rub hands together until dry.
  • Super vise children under 6 years of age when using this product to avoids wallowing.

Other information

SPL UNCLASSIFIED SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Carbomer,hydrogen peroxide,fragance,and demineralized water.

Package Labeling:3.78L

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Box3Box3

Package Labeling:208 L

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Box4Box4

Products#

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DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79324-00179324-001-01, 79324-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
0799172d-d3e9-d58e-e063-6394a90aea97aae36ab8-d07e-c923-e053-2995a90a0a572023-10-13WarningsExact identifier
spl set id: aae36ab8-d07e-c923-e053-2995a90a0a57

Reported adverse events (FAERS/openFDA)#

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