FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Rapid Care, Inc
Effective date
2020-04-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:35:27

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

for handwashing to decrease bacteria on skin without soap and water. recommended for repeated use

Dosage and administration

wet hands and wrists thoroughly with product and allow to dry without wiping children under 6 years of age should be supervised while using this product

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • for handwashing to decrease bacteria on skin without soap and water.
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flames.

Do not use in the eyes. If this happens, rinse thoroughly with water.

Use with caution if allergic to alcohol.

Do not use

OTC - DO NOT USE SECTION

in the eyes. If this happens, rince thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

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 ingested get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands and wrists thoroughly with product and allow to dry without wiping
  • children under 6 years of age should be supervised while using this product

Inactive ingredient

INACTIVE INGREDIENT SECTION

carbomer, favor, glycerine, triclosen, triethanolamine, purified water

RapidCare - Hand Sanitizer - 1pc

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand SanitizerHand Sanitizer

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73659-00473659-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
CARBOMER 9404Q93RCW27EIACT
GLYCERINPDC6A3C0OXIACT
TRICLOSAN4NM5039Y5XIACT

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
ce589535-9e96-7959-e053-2a95a90a619aa3783567-cfaf-e690-e053-2995a90a657f2021-10-14WarningsExact identifier
spl set id: a3783567-cfaf-e690-e053-2995a90a657f

Reported adverse events (FAERS/openFDA)#

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