FDA.reportPublic FDA data

Appeal Alcohol Foaming Hand Sanitizer

Manufacturer
SC Johnson Professional USA, Inc. | SC Johnson Professional CA Inc.
Effective date
2024-12-16
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 20:45:44

Label at a glance#

ProductAppeal Alcohol Foaming Hand Sanitizer
Active ingredientAlcohol
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethyl Alcohol 70% ww

OTC - PURPOSE SECTION

Purpose

Antibacterial

INDICATIONS & USAGE SECTION

Uses

For hand sanitizing to reduce bacteria on the skin

WARNINGS SECTION

Warnings

For external use only

Flammable: Keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes.  In case of eye contact, flush with water.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

Apply one shot of foaming sanitizer to dry hands

Rub into skin

No rinsing required

INACTIVE INGREDIENT SECTION

Inactive ingredients

Water, Bis-PEG-12 Dimethicone, Behentrimonium Chloride, PEG-200 Hydrogenated Glyceryl Palmate, PEG-7 Glyceryl Cocoate, Coco-Glucoside, Glyceryl Oleate, Dihydroxypropyl PEG-5 Linoleammonium Chlroide

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

container labelcontainer label

APP17102

102668

appeal Alcohol Foaming Hand Sanitizer

Certified EcoLogo

Certified Instant Hand Antiseptic CCD-170

1 Liter

33.8 Fluid Ounces

Made in Canada by Deb

deb foam technolody

Distributed exclusively by:

Interline Brands

Jacksonville, FL  32207

www.AppealProducts.com

Rev. 05-12

01830

container labelcontainer label

container labelcontainer label

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11084-702APPEAL ALCOHOL FOAMING HAND SANITIZER (ETHYL ALCOHOL) LIQUID [SC JOHNSON PROFESSIONAL USA, INC.]7Legacy NDC20241218_6b35e9f7-1e3e-41c6-9250-e1ce744b302e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AlcoholACTIVE INGREDIENT3K9958V90M3
AlcoholACTIVE MOIETY3K9958V90M3
BEHENTRIMONIUM CHLORIDEINACTIVE INGREDIENTX7GNG3S47T3
COCO GLUCOSIDEINACTIVE INGREDIENTICS790225B3
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDEINACTIVE INGREDIENT0Y0NQR2GH13
DIMETHICONEINACTIVE INGREDIENT92RU3N3Y1O3
GLYCERYL COCOATEINACTIVE INGREDIENTWVK1CT59943
GLYCERYL MONOOLEATEINACTIVE INGREDIENT4PC054V79P3
PEG-200 DILAURATEINACTIVE INGREDIENTTWV5J70L883
WATERINACTIVE INGREDIENT059QF0KO0R3

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
11084-70211084-702-27

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
Alcohol3K9958V90MACTIB
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE0Y0NQR2GH1IACT
BEHENTRIMONIUM CHLORIDEX7GNG3S47TIACT
DIMETHICONE92RU3N3Y1OIACT
COCO-GLUCOSIDEICS790225BIACT
PEG-200 DILAURATETWV5J70L88IACT
GLYCERYL COCOATEWVK1CT5994IACT
GLYCERYL MONOOLEATEC4YAD5F5G6IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 7 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
GLYCERYL MONOOLEATEGLYCERYL OLEATE4PC054V79PTABLET / ORAL3 mgExact identifier — unii candidate
7 equally ranked IID candidates
GLYCERYL MONOOLEATEGLYCERYL OLEATE4PC054V79PPOWDER, FOR SUSPENSION / ORALNAExact identifier — unii candidate
7 equally ranked IID candidates
GLYCERYL MONOOLEATEGLYCERYL OLEATE4PC054V79PGEL / TOPICAL1 %w/wExact identifier — unii candidate
7 equally ranked IID candidates
GLYCERYL MONOOLEATEGLYCERYL OLEATE4PC054V79PSPRAY / TOPICAL0.95 %w/wExact identifier — unii candidate
7 equally ranked IID candidates
GLYCERYL MONOOLEATEGLYCERYL OLEATE4PC054V79PFILM, EXTENDED RELEASE / TRANSDERMAL18.8 mgExact identifier — unii candidate
7 equally ranked IID candidates
GLYCERYL MONOOLEATEGLYCERYL OLEATE4PC054V79PCREAM, AUGMENTED / TOPICAL3.5 %w/wExact identifier — unii candidate
7 equally ranked IID candidates
GLYCERYL MONOOLEATEGLYCERYL OLEATE4PC054V79PCAPSULE / ORALNAExact identifier — unii candidate
7 equally ranked IID candidates

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
8ec64608-2130-410c-87cb-bd8bc33244246b35e9f7-1e3e-41c6-9250-e1ce744b302e2024-12-16WarningsExact identifier
spl id: 8ec64608-2130-410c-87cb-bd8bc3324424
spl set id: 6b35e9f7-1e3e-41c6-9250-e1ce744b302e

Reported adverse events (FAERS/openFDA)#

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