SolGreat Alcohol-Free Hand Sanitizer

Manufacturer
PANATURAL USA, INC.
Effective date
2020-04-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:08:24

Label at a glance#

ProductSolGreat Alcohol-Free Hand Sanitizer
Active ingredientBenzalkonium Chloride
Label structure9 sections

Indications and uses

hand sanitizer to help decrease bacteria on the skin, when water, soap & towel are not available. recommended for repeated use

Dosage and administration

place enough product into your palms and thoroughly spread on both hands. rub into skin until dry.

Label contents#

Full prescribing information#

Active lngredient  

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride

Purpose 

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

  • hand sanitizer to help decrease bacteria on the skin, when water, soap & towel are not available.
  • recommended for repeated use

Warnings  

WARNINGS SECTION


For external use only.

Flammable. Keep away from fire or flame.

Do not apply around eyes. Do not use in ears & mouth.

When using this product, avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

Directions

DOSAGE & ADMINISTRATION SECTION

  • place enough product into your palms and thoroughly spread on both hands.
  • rub into skin until dry.

Inactive ingredients 

INACTIVE INGREDIENT SECTION

BUTYLENE GLYCOL, CITRIC ACID, DIAZOLIDINYL UREA, HYDROXYETHYCELLULOSE, PEG-40 HYDROGENATE CASTOR OIL, PROPYLENE GLYCOL, WATER.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children must be supervised in use of this product

Products Label-237mL SolGreat Alcohol-Free Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Product Label- 500mL SolGreat Alcohol-Free Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1098199benzalkonium chloride 0.13 % Topical GelPSN2
1098199benzalkonium chloride 0.0013 MG/MG Topical GelSCD2
1098199benzalkonium chloride 0.13 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73913-004-012022-01-28C16284748780-1d6a99b39-8ab2-a426-e053-dadaa90af4c2SolGreat Alcohol-Free Hand Sanitizer
73913-004-022022-01-28C16284748780-1d6a99b39-8ab2-a426-e053-dadaa90af4c2SolGreat Alcohol-Free Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73913-004-01SolGreat Alcohol-Free Hand Sanitizer237 mL in 1 BOTTLE, PLASTICGEL2372
73913-004-02SolGreat Alcohol-Free Hand Sanitizer500 mL in 1 BOTTLE, PLASTICGEL5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73913-004SOLGREAT ALCOHOL-FREE HAND SANITIZER (BENZALKONIUM CHLORIDE) GEL [PANATURAL USA, INC.]2Legacy NDC, 2 package rows20200428_db7d0307-d754-428c-b483-eefd1e2ea9d4.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73913-00473913-004-01, 73913-004-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
9aeb2181-41d9-4adb-9563-6f52d020b9f0db7d0307-d754-428c-b483-eefd1e2ea9d42020-04-22WarningsExact identifier
spl id: 9aeb2181-41d9-4adb-9563-6f52d020b9f0
spl set id: db7d0307-d754-428c-b483-eefd1e2ea9d4

Reported adverse events (FAERS/openFDA)#

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