FDA.reportPublic FDA data

Blumen Advance Hand Sanitizer Wipes Clear

Manufacturer
4E BRANDS NORTHAMERICA, LLC | HangZhou YangYi Daily Cosmetics Technology Co., Ltd.
Effective date
2020-06-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:23:08

Label at a glance#

ProductBlumen Advance Hand Sanitizer Wipes Clear
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin

Dosage and administration

- Wet hands thoroughly with product and allow to dry - Discard wipes in trash receptacle after use. Do not flush - Children under 6 years of age should be supervised when using this product

Label contents#

Full prescribing information#

Activeingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial 

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

  • 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

irritation or rash apperars 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

- Wet hands thoroughly with product and allow to dry

- Discard wipes in trash receptacle after use. Do not flush

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Ethylhexylglycerin, Phenoxyethanol, Didecyldimonium Chloride, Propylene Glycol, Parfum (Fragrance), Aloe Barbadensis Leaf Extract (Aloe Vera), Tocopheryl Acetate (Vitamin E).

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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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
70074-02570074-025-00

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
PHENOXYETHANOLHIE492ZZ3TIACT
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
d2cbf516-496a-2ca2-e053-2995a90a99928bb32f35-0d12-40af-b6a5-4a5638bc79322021-12-10WarningsExact identifier
spl set id: 8bb32f35-0d12-40af-b6a5-4a5638bc7932

Reported adverse events (FAERS/openFDA)#

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