Advanced Hand Sanitizer

Manufacturer
Flex Beauty Labs, LLC
Effective date
2018-05-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:55:27

Label at a glance#

ProductAdvanced Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand Santizer to help reduce bacteria on skin that may cause disease.

Dosage and administration

. Place enough Product in your palm to thoroughtly spread on both hands and rub into the skin until dry. . Children under 6 years of age should be supervised when using this product.

Storage and handling

. Store below 106℉. (41℃)

Label contents#

Full prescribing information#

Drug Facts Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62.0%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INSTRUCTIONS FOR USE SECTION

Hand Santizer to help reduce bacteria on skin that may cause disease.

Warnings

WARNINGS SECTION

Flammable. Keep away from heat or flame.

For external use only.

When using this product,

DOSAGE & ADMINISTRATION SECTION

do not use in or near the eyes. In case of contact, rinse eyes thoroughtly with water. Stop use and ask doctor if irritation or rash appears and lasts. Keep out of reach for children.

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

Directions:

INDICATIONS & USAGE SECTION

. Place enough Product in your palm to thoroughtly spread on both hands and rub into the skin until dry.

. Children under 6 years of age should be supervised when using this product.

Other Information:

STORAGE AND HANDLING SECTION

. Store below 106℉. (41℃)

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water (Aqua), Aloe Vera Leaf , Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E), Triethanolamine, 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

advance hand sanitizeradvance hand sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
247835ethanol 62 % Topical SolutionPSN2
247835ethanol 0.62 ML/ML Topical SolutionSCD2
247835ethanol 62 % Topical SolutionSY2
247835ethyl alcohol 62 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72308-001-012020-01-31C16284748780-19d75b9d0-7d98-f424-e053-dadaa90a57ce5a5562eb-9864-46cf-a35e-d11741166f53

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72308-001-01Advanced Hand Sanitizer295 mL in 1 BOTTLE, PLASTICLIQUID2952

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72308-001ADVANCED HAND SANITIZER (HAND SANITIZER) LIQUID [FLEX BEAUTY LABS, LLC]2Legacy NDC, 1 package rows20180507_5a5562eb-9864-46cf-a35e-d11741166f53.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
72308-00172308-001-01

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
6b9e574c-36b7-553a-e053-2991aa0ae65b5a5562eb-9864-46cf-a35e-d11741166f532018-05-07WarningsExact identifier
spl id: 6b9e574c-36b7-553a-e053-2991aa0ae65b
spl set id: 5a5562eb-9864-46cf-a35e-d11741166f53

Reported adverse events (FAERS/openFDA)#

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