SolGreat Instant 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 23:08:13

Label at a glance#

ProductSolGreat Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure11 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

Ethyl Alcohol

Purpose

OTC - PURPOSE SECTION

Antiseptic 

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.

Inactives 

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf juice, carbomer, triethanolamine, 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

  • store below 1100F (43oC).
  • may discolor certain fabrics or surfaces.

Product Labe-60mL SolGreat Alcohol Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60mL60mL

Product Label-237mL SolGreat Alcohol Hand Sanitizerr

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

237mL237mL

Product Label 500mL SolGreat Alcohol Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500mL500mL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN2
581662ethanol 0.7 ML/ML Topical GelSCD2
581662ethanol 70 % Topical GelSY2
581662ethyl alcohol 70 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73913-001-01SolGreat Instant Hand Sanitizer60 mL in 1 BOTTLEGEL602
73913-001-02SolGreat Instant Hand Sanitizer237 mL in 1 BOTTLEGEL2372
73913-001-03SolGreat Instant Hand Sanitizer500 mL in 1 BOTTLEGEL5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73913-001SOLGREAT INSTANT HAND SANITIZER (ETHYL ALCOHOL) GEL [PANATURAL USA, INC.]2Legacy NDC, 3 package rows20200428_9c734b13-ccaa-4cb6-95c8-7227b6db5f6c.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
73913-00173913-001-01, 73913-001-02, 73913-001-03

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 · Source PDF

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
65e7e880-494c-4af3-ab29-facb950948e49c734b13-ccaa-4cb6-95c8-7227b6db5f6c2020-04-22WarningsExact identifier
spl id: 65e7e880-494c-4af3-ab29-facb950948e4
spl set id: 9c734b13-ccaa-4cb6-95c8-7227b6db5f6c

Reported adverse events (FAERS/openFDA)#

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