Spector Scientific Lab Hand Sanitizer Soothing Gel Infused With Aloe Vera

Manufacturer
Spector Scientific Laboratory, Inc
Effective date
2022-10-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:51:22

Label at a glance#

ProductSpector Scientific Lab Hand Sanitizer Soothing Infused With Aloe Vera
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

USE

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

WARNINGS

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only.

When using this product 

OTC - WHEN USING SECTION

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask doctor if

OTC - STOP USE SECTION

irritation or rash appears and lasts.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • Put enough product in your palm to cover hands and rub hands together until dry.
  • Children under 6 years of age should be supervised when using this product.

OTHER INFORMATION

SPL UNCLASSIFIED SECTION

  • Store below 110°F (43°C).
  • May discolor certain fabric surfaces.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water/Aqua, Isopropyl Alcohol, Glycerin, Carbomer, Aminomethyl Propanol, Aloe Barbadensis Leaf Juice.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabelLabel2Label2

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78943-00378943-003-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
eb506e9c-abe7-357e-e053-2995a90a9533a8b15217-cccc-2260-e053-2995a90a709d2022-10-18WarningsExact identifier
spl id: eb506e9c-abe7-357e-e053-2995a90a9533
spl set id: a8b15217-cccc-2260-e053-2995a90a709d

Reported adverse events (FAERS/openFDA)#

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