FDA.reportPublic FDA data

7 Select Instant Hand Sanitizer

Manufacturer
7-Eleven Inc | Delta Kozmetik Sanayi Ve Ticaret-Selim Yesil
Effective date
2021-01-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:56:13

Label at a glance#

Product7 Select Instant Hand Sanitizer with Vitamin E and Moisturizers
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

■ place enough product in your palm to thoroughly spread on both hands and rub into the skin 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% v/v

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 and 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 a doctor if

OTC - STOP USE SECTION

■ if 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

■ place enough product in your palm to thoroughly 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

SPL UNCLASSIFIED SECTION

​■ store below 106F (41C) ■ may discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, propylene glycol, acrylates/c10-30 alkyl acrylate crosspolymer, isopropyl alcohol, aminomethylpropanol, isopropyl myristate, caprylyl glycol, phenoxyethanol, fragrance, tocopherol acetate

Questions or Comments

OTC - QUESTIONS SECTION

1-844-428-2538

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10202-10010202-100-02, 10202-100-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALCOHOL3K9958V90MACTIB
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
CAPRYLYL GLYCOL00YIU5438UIACT
PHENOXYETHANOLHIE492ZZ3TIACT
AMINOMETHYLPROPANOLLU49E6626QIACT

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
feb8cebe-c218-7616-e053-6394a90a30673fc81cfb-c32b-51d3-e054-00144ff8d46c2023-06-22WarningsExact identifier
spl set id: 3fc81cfb-c32b-51d3-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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