FDA.reportPublic FDA data

angel of mine

Manufacturer
Greenbrier International, 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 22:56:18

Label at a glance#

Productangel of mine FOAMING HAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Dosage and administration

■ wet hands thoroughly with product and allow to dry without wiping ■ for children under 6, use only under adult supervision

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only, hands only

When using this product

OTC - WHEN USING SECTION

■ avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water ■ avoid contact with broken skin

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ irritation or redness develops ■ condition persists for more than 72 hours

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 without wiping ■ for children under 6, use only under adult supervision

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, cetrimonium chloride, disodium cocoamphodiacetate, PEG-12 dimethicone, citrus reticulata X C sinensis peel extract, tocopheryl acetate, methylchloroisithiazolinone, methylisothiazolinone

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
33992-1450-82023-01-30C16284748780-1f386c649-e87d-0266-e053-dadaa90a7c1aangel of mine Foaming Hand Sanitizer

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
33992-1450ANGEL OF MINE FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [GREENBRIER INTERNATIONAL, INC]2Legacy NDC20210116_a3bf282b-a4b7-464d-e053-2a95a90a000d.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
33992-145033992-1450-8

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
METHYLISOTHIAZOLINONE229D0E1QFAIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
WATER059QF0KO0RIACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
PEG-12 DIMETHICONEZEL54N6W95IACT
TANGERINE PEELJU3D414057IACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT

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
b8f42133-645f-3668-e053-2995a90a1805a3bf282b-a4b7-464d-e053-2a95a90a000d2021-01-15WarningsExact identifier
spl id: b8f42133-645f-3668-e053-2995a90a1805
spl set id: a3bf282b-a4b7-464d-e053-2a95a90a000d

Reported adverse events (FAERS/openFDA)#

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