Hand Sanitizer FOREST SCENT

Manufacturer
GREAT EAGLE GROUP INC | NICE ENTERPRISE CO LTD
Effective date
2020-03-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:04:38

Label at a glance#

ProductHand Sanitizer FOREST SCENT
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available. Recomended for repeated use.

Dosage and administration

Pump as needed in to your palms and throughly spread on both hand. 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 reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Recomended for repeated use.

Warnings  

WARNINGS SECTION

  • For external use only
  • Flammable
  • Keep away from heat and flame.
  •  Do not use in ear , mouth OR eyes.
  • When using this product

  Avoid contact with eyes. In case of eye contact, flush with water.

  • Keep out of reachof children.

If swallowed, seek medical attention immidately.

Directions

DOSAGE & ADMINISTRATION SECTION

Pump as needed in to your palms and throughly spread on both hand.

Rub into skin until dry.

Inactives 

INACTIVE INGREDIENT SECTION

Deionized Water, 
D-Panthenol
Fragrance
o-Cymen-5-ol
Thymus Vulgaris (Thyme) Flower/Leaf Extract

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Product Label  

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

product-labelproduct-label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286295ethanol 75 % Topical SprayPSN1
2286295ethanol 0.75 ML/ML Topical SpraySCD1
2286295ethanol 75 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73861-001-012021-07-23C16284748780-1c7ccaba7-28a1-fd44-e053-dadaa90aa01bHand Sanitizer FOREST SCENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73861-001-01Hand Sanitizer FOREST SCENT145 mL in 1 BOTTLESPRAY1451

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73861-001HAND SANITIZER FOREST SCENT (ETHYL ALCOHOL) SPRAY [GREAT EAGLE GROUP INC]1Legacy NDC, 1 package rows20200401_bbaa8311-74bb-4cf3-b5b8-ced19836519c.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
73861-00173861-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
b7cd78ef-9f77-420e-a642-462b1ff6ad4cbbaa8311-74bb-4cf3-b5b8-ced19836519c2020-03-27WarningsExact identifier
spl id: b7cd78ef-9f77-420e-a642-462b1ff6ad4c
spl set id: bbaa8311-74bb-4cf3-b5b8-ced19836519c

Reported adverse events (FAERS/openFDA)#

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