FDA.reportPublic FDA data

Personal CARE Foaming Hand Sanitizer

Manufacturer
Delta Brands Inc
Effective date
2023-06-22
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:29:42

Label at a glance#

ProductPersonal CARE Foaming Hand Sanitizer Mint Lemon
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

to reduce bacteria on the skin.

Dosage and administration

■wet hands thoroughly with product and alllow 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

Uses

INDICATIONS & USAGE SECTION

to reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only, hands only

When using this product

OTC - WHEN USING SECTION

■ avoid contact with 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 alllow to dry without wiping ■for children under 6, use only under adult supervision

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, cetrimonium chloride, disodium cocoaphodiacetate, PEG-40 hydrogenated castor oil,PEG-12 dimethicone, methylchloroisothiazolinone, methylisothiazolinone, citrus limon (lemon) peel oil, mentha viridis (spearmint) leaf oil, cymbopogon schoenanthus oil, tocopheryl acetate

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 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
20276-14120276-141-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
LEMON OILI9GRO824LLIACT
MENTHA SPICATA OILC3M81465G5IACT
WATER059QF0KO0RIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
CYMBOPOGON SCHOENANTHUS OILXE7K568ILOIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
PEG-12 DIMETHICONE (300 CST)ZEL54N6W95IACT
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
feba4ab4-4552-de12-e053-6394a90a4bc69dc44ebd-c45f-68e7-e053-2a95a90a3a2e2023-06-22WarningsExact identifier
spl id: feba4ab4-4552-de12-e053-6394a90a4bc6
spl set id: 9dc44ebd-c45f-68e7-e053-2a95a90a3a2e

Reported adverse events (FAERS/openFDA)#

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