FDA.reportPublic FDA data

SolGreat Alcohol-Free Foaming Hand Sanitizer

Manufacturer
PANATURAL USA, INC. | Hefei Yatai Daily-Use Chemical Industry Co., Ltd
Effective date
2020-03-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:04:26

Label at a glance#

ProductSolGreat Alcohol-Free Foaming Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

hand sanitizer to help reduce bacteria on the skin that could cause disease. recommended for repeated use.

Dosage and administration

place enough product in your palm to thoroughly cover your hands. rub hands together until dry. children under 6 years of age should be supervised when using this product.

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 reduce bacteria on the skin that could cause disease.
  • recommended for repeated use.

Warnings  

WARNINGS SECTION

For external use only.

When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly 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 in your palm to thoroughly cover your hands.
  • rub hands together until dry.
  • children under 6 years of age should be supervised when using this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

cetrimonium chloride citric acid, cocamidopropyl betaine, cocamidopropylamine oxide, glycerin, propylene glycol, tocopheryl acetate, water.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


Children must be supervised in use of this product.

Other information

SPL UNCLASSIFIED SECTION

To prevent discoloration, avoid contact with clothing.

Product Label - 60 mL SolGreat Alcohol-Free Hand Sanitizer Spray

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60mL60mL

Product  Label- 354mL SolGreat Alcohol-Free Foaming Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

354ml354ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039012benzalkonium chloride 0.13 % Topical SprayPSN1
1039012benzalkonium chloride 1.3 MG/ML Topical SpraySCD1
1039012benzalkonium chloride 0.13 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73913-002-012022-01-28C16284748780-1d6a99b39-ef37-a426-e053-dadaa90af4c2SolGreat Alcohol-Free Hand Sanitizer
73913-002-022022-01-28C16284748780-1d6a99b39-ef37-a426-e053-dadaa90af4c2SolGreat Alcohol-Free Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73913-002-01SolGreat Alcohol-Free Foaming Hand Sanitizer60 mL in 1 BOTTLESPRAY601
73913-002-02SolGreat Alcohol-Free Foaming Hand Sanitizer354 mL in 1 BOTTLESPRAY3541

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73913-002SOLGREAT ALCOHOL-FREE FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) SPRAY [PANATURAL USA, INC.]1Legacy NDC, 2 package rows20200331_baf6ffa6-721e-444c-bbcf-5b6164ab219b.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73913-00273913-002-01, 73913-002-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
COCAMIDOPROPYLAMINE OXIDEM4SL82J7HKIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT

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
3d005f5e-06da-429d-84ca-18140440abc7baf6ffa6-721e-444c-bbcf-5b6164ab219b2020-03-27WarningsExact identifier
spl id: 3d005f5e-06da-429d-84ca-18140440abc7
spl set id: baf6ffa6-721e-444c-bbcf-5b6164ab219b

Reported adverse events (FAERS/openFDA)#

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