FDA.reportPublic FDA data

CLIP Hand Sanitizer

Manufacturer
Shalom, S.A.
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:17:27

Label at a glance#

ProductCLIP Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

To help reduce bacteria on the skin that could cause disease. Recommended for repeated use.

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient Ethyl alcohol 60% v/v

OTC - ACTIVE INGREDIENT SECTION

354 ml rear label354 ml rear label

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

To help reduce bacteria on the skin that could cause disease. Recommended for repeated use.

Warnings

WARNINGS SECTION

Flammable. Keep away from source of heat, fire or flame. For external use only.

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes. I contact occurs, rinse thoroughly with water. Avoid contact with broken skin.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Irritation or redness develops 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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, carbomer, glycerine, triethanolamine, cucumis sativus extract, camellia sinensis (green tea) infusion.

Other information

OTHER SAFETY INFORMATION

Store at a temperature below 110ºF (43ºC). May discolor some fabric.

CLIP Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

354 ml NDC: 78910-001-01

Advanced. Kills up to 99% of bacteria, germs, and other microorganisms. Refreshing gel with cucumber extract and green tea infusion.

354 ml label354 ml label

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
78910-00178910-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER 9404Q93RCW27EIACT
GLYCERINPDC6A3C0OXIACT
CUCUMBER JUICE61845009SPIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
TROLAMINE9O3K93S3TKIACT
TEA LEAF OILVC855RRT77IACT

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
e9c9474d-0630-6b58-e053-2a95a90a5d10aa382c9d-a425-5530-e053-2a95a90a08ba2022-09-28WarningsExact identifier
spl set id: aa382c9d-a425-5530-e053-2a95a90a08ba

Reported adverse events (FAERS/openFDA)#

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