FDA.reportPublic FDA data

Insignia Instant Hand Sanitizer

Manufacturer
Yiwu Story of Love Cosmetic Co., Ltd
Effective date
2020-06-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:16:45

Label at a glance#

ProductInsignia Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Wet hands thoroughly with product and rub until dry without wiping For children under 6, use only under adult supervision Not recommended for infants

Storage and handling

Do not store above 40C (104F) May discolor wood or fabrics Harmful to wood finishes or plastics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 80% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could cause disease

Recommended for repeated use

To use anywhere without water

Warnings

WARNINGS SECTION

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

Discontinue if skin becomes irritated and ask a doctor

OTC - WHEN USING SECTION

When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water.

Do not inhale or ingest

Avoid contact with broken skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingest, seek professional assist or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and rub until dry without wiping
  • For children under 6, use only under adult supervision
  • Not recommended for infants

Other information

STORAGE AND HANDLING SECTION

  • Do not store above 40C (104F)
  • May discolor wood or fabrics
  • Harmful to wood finishes or plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Carbomer, Triethanolamine, Glycerin, PEG-7 glyceryl CoCoate, Water, Parfum (Fragrance), Aloe barbadensis leaf extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN1
1039339ethanol 0.8 ML/ML Topical SolutionSCD1
1039339ethanol 80 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75410-003-012022-01-28C16284748780-1d6a99b39-a7ed-a426-e053-dadaa90af4c2ac1d036e-f895-45c3-9f2c-00bd374dab6a
75410-003-022022-01-28C16284748780-1d6a99b39-a7ed-a426-e053-dadaa90af4c2ac1d036e-f895-45c3-9f2c-00bd374dab6a
75410-003-032022-01-28C16284748780-1d6a99b39-a7ed-a426-e053-dadaa90af4c2ac1d036e-f895-45c3-9f2c-00bd374dab6a
75410-003-042022-01-28C16284748780-1d6a99b39-a7ed-a426-e053-dadaa90af4c2ac1d036e-f895-45c3-9f2c-00bd374dab6a
75410-003-052022-01-28C16284748780-1d6a99b39-a7ed-a426-e053-dadaa90af4c2ac1d036e-f895-45c3-9f2c-00bd374dab6a
75410-003-062022-01-28C16284748780-1d6a99b39-a7ed-a426-e053-dadaa90af4c2ac1d036e-f895-45c3-9f2c-00bd374dab6a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75410-003-01Insignia Instant Hand Sanitizer50 mL in 1 BOTTLESOLUTION501
75410-003-02Insignia Instant Hand Sanitizer60 mL in 1 BOTTLESOLUTION601
75410-003-03Insignia Instant Hand Sanitizer100 mL in 1 BOTTLESOLUTION1001
75410-003-04Insignia Instant Hand Sanitizer250 mL in 1 BOTTLESOLUTION2501
75410-003-05Insignia Instant Hand Sanitizer500 mL in 1 BOTTLESOLUTION5001
75410-003-06Insignia Instant Hand Sanitizer1000 mL in 1 BOTTLESOLUTION10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75410-003INSIGNIA INSTANT HAND SANITIZER (ALCOHOL) SOLUTION [YIWU STORY OF LOVE COSMETIC CO., LTD]1Legacy NDC, 6 package rows20200609_ac1d036e-f895-45c3-9f2c-00bd374dab6a.zip

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
75410-00375410-003-01, 75410-003-02, 75410-003-03, 75410-003-04, 75410-003-05, 75410-003-06

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
GLYCERINPDC6A3C0OXIACT
CARBOMER 934Z135WT9208IACT
TRIETHANOLAMINE SULFATEMV1V89M17OIACT
PEG-7 GLYCERYL COCOATEVNX7251543IACT
ALOE VERA LEAFZY81Z83H0XIACT
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
a7999ec5-effc-28cb-e053-2a95a90aa43cac1d036e-f895-45c3-9f2c-00bd374dab6a2020-06-08WarningsExact identifier
spl id: a7999ec5-effc-28cb-e053-2a95a90aa43c
spl set id: ac1d036e-f895-45c3-9f2c-00bd374dab6a

Reported adverse events (FAERS/openFDA)#

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