FDA.reportPublic FDA data

Hand Sanitizer 70 Alcohol

Manufacturer
Servi Quim de Monterrey, S.A. de C.V.
Effective date
2023-10-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:58:15

Label at a glance#

ProductHand Sanitizer 70 Alcohol
Active ingredientALCOHOL
Label structure7 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 70% 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:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Box2Box2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79324-000-012025-11-10C16284748780-11030e365-17af-111a-e063-dadaa90a10e2Hand Sanitizer 70% Alcohol
79324-000-012024-07-30C16284748780-11030e365-17af-111a-e063-dadaa90a10e2Hand Sanitizer 70% Alcohol
79324-000-012024-01-30C16284748780-11030e365-17af-111a-e063-dadaa90a10e2Hand Sanitizer 70% Alcohol

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79324-000HAND SANITIZER 70 ALCOHOL (ALCOHOL) GEL [SERVI QUIM DE MONTERREY, S.A. DE C.V.]2Legacy NDC20231030_aae3d7c4-2809-8f7b-e053-2995a90a52a4.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79324-00079324-000-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
WATER059QF0KO0RIACT
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
4342da82-2a97-58ff-e063-6294a90ab782aae3d7c4-2809-8f7b-e053-2995a90a52a42025-11-10WarningsExact identifier
spl set id: aae3d7c4-2809-8f7b-e053-2995a90a52a4

Reported adverse events (FAERS/openFDA)#

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