Every Fresh Hand Sanitizer

Manufacturer
TSM ITHALAT IHRACAT SANAYI VE DIS TICARET LIMITED SIRKETI
Effective date
2020-12-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:35:30

Label at a glance#

ProductEvery Fresh Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

To help reduce bacteria on the skin For use when soap and water are not available

Dosage and administration

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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol, 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • To help reduce bacteria on the skin
  • For use when soap and water are not available

Warnings

WARNINGS SECTION

For external use only. Flammable, keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if significant irritation or sensitization develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

-Put enough product on your palm to cover hands and rub your hands together until dry.

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

Other Information

SPL UNCLASSIFIED SECTION

Store below 43°C (110°F)

May discolor certain fabrics

Inactive Ingredients

INACTIVE INGREDIENT SECTION

carbomer, aloe barbadensis leaf juice, aminomethyl propanol, glycerin, water, tocopheryl acetate (Vit E).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

22

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN3
581662ethanol 0.7 ML/ML Topical GelSCD3
581662ethanol 70 % Topical GelSY3
581662ethyl alcohol 70 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76772-014-052023-01-30C16284748780-1f386c649-d1e3-0266-e053-dadaa90a7c1aEvery Fresh Hand sanitizer
76772-014-232023-01-30C16284748780-1f386c649-d1e3-0266-e053-dadaa90a7c1aEvery Fresh Hand sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76772-014-05Every Fresh Hand Sanitizer148 mL in 1 BOTTLEGEL1483
76772-014-23Every Fresh Hand Sanitizer236 mL in 1 BOTTLEGEL2363

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76772-014EVERY FRESH HAND SANITIZER (ETHYL ALCOHOL) GEL [TSM ITHALAT IHRACAT SANAYI VE DIS TICARET LIMITED SIRKETI]3Legacy NDC, 2 package rows20201218_ad664489-1ff0-a77f-e053-2a95a90a06cc.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76772-01476772-014-05, 76772-014-23

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
b6af3459-6464-254b-e053-2a95a90ab670ad664489-1ff0-a77f-e053-2a95a90a06cc2020-12-17WarningsExact identifier
spl id: b6af3459-6464-254b-e053-2a95a90ab670
spl set id: ad664489-1ff0-a77f-e053-2a95a90a06cc

Reported adverse events (FAERS/openFDA)#

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