CELAVI HAND SANITIZING WET WIPES

Manufacturer
BLANC MER | FIRSTCHAM CO., LTD
Effective date
2020-12-10
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:34:55

Label at a glance#

ProductCELAVI HAND SANITIZING WET WIPES
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

■instant healthcare personnel hand antiseptic to reduce bacteria that potentially can cause disease ■instant hand antiseptic to decrease bacteria on the skin

Dosage and administration

■ Scrub and wipe off the hand and skin, which are used individually or if necessary.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Glycerin, Sodium benzoate, Polysorbate 20, Disodium EDTA, Phenoxyethanol, Tocopheryl acetate, Citric acid

PURPOSE

OTC - PURPOSE SECTION

antiseptic

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Uses

INDICATIONS & USAGE SECTION

■instant healthcare personnel hand antiseptic to reduce bacteria that potentially can cause disease

■instant hand antiseptic to decrease bacteria on the skin

WARNINGS

WARNINGS SECTION

Warnings

For external use only


When using this product
■ if following abnormal symptoms persist, discontinue use
Irritation around the eyes, ears, mucous membranes, including the mouth, under the skin irritation and rashes
■ Stop immediately and consult a doctor if you experience
1) Hypersensitivity symptoms such as erythema, itching and dermatitis.
2) Skin Irritation
3) Following Instructions when using medication
(1) For external use only (Do not use internally)
(2) Avoid getting into the eyes (if contact occurs, wash well with clean water)
■ When used repeatedly in the same area, skin irritation may occur.
■Do not use the product for a long time in the same area as swelling, inflammation or sickness may occur due to absorption through the skin.
It is not recommended to use this one areas that have been medically treated with a cast or bandage.
■Do not use in combination with soap or antibacterial cleansing agents.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Scrub and wipe off the hand and skin, which are used individually or if necessary.

Other information

OTHER SAFETY INFORMATION

■ Read the directions and warnings before use

■ Avoid freezing and excessive heat above 40 ℃ (104 ℉)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of containerImage of container

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038856benzalkonium Cl 0.1 % Medicated PadPSN3
1038856benzalkonium chloride 1 MG/ML Medicated PadSCD3
1038856benzalkonium chloride 0.1 % Medicated WipesSY3
1038856benzalkonium chloride 0.1 % Topical SwabSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75770-010-012022-01-28C16284748780-1d6a99b39-80a5-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75770-010-01CELAVI HAND SANITIZING WET WIPES162 g in 1 CONTAINERLIQUID1623

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75770-010CELAVI HAND SANITIZING WET WIPES (BENZALKONIUM CHLORIDE) LIQUID [BLANC MER]3Legacy NDC, 1 package rows20201211_42051b24-d044-4aaf-930c-d64a95e7ebe1.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75770-01075770-010-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

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
7b059ae9-1191-4002-b12b-252d38f906e542051b24-d044-4aaf-930c-d64a95e7ebe12020-12-10WarningsExact identifier
spl id: 7b059ae9-1191-4002-b12b-252d38f906e5
spl set id: 42051b24-d044-4aaf-930c-d64a95e7ebe1

Reported adverse events (FAERS/openFDA)#

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