FDA.reportPublic FDA data

Odorless Hand Sanitizer Foam

Manufacturer
Tinks | American Accessories of Pensacola, Inc. | Tropical Products, Inc
Effective date
2010-08-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:26:00

Label at a glance#

ProductOdorless Hand Sanitizer Foam
Active ingredientBenzalkonium Chloride
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Benzalkonium Chloride 0.1%

OTC - PURPOSE SECTION

Purpose

Antimicrobial

INDICATIONS & USAGE SECTION

Uses

For Hand sanitizing to decrease bacteria on the skin

Recommended for repeated uses

WARNINGS SECTION

Warnings

For external use only

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions

Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands together briskly until dry.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Water, Aloe Vera*, Vitamin E*, Green Tea Extract*, Dihydroxypropyl PEG-5 Linoleamonium Chloride, Glycereth-2 Cocoate, Behentrimonium Chloride, Dihydroxyethyl Cocamine Oxide.

*Skin Conditioner

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Tink's

Odorless Hand

Sanitizer Foam

Sanitize your hands after field dressing

Alcohol Free

Kills 99.99% of Harmful Germs and Bacteria

Rinse free formula

Enriched with moisturizing agents

tinks69.com

5 FL. OZ. (150 ML)

container labelcontainer label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN1
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD1
1038799benzalkonium chloride 0.1 % Topical FoamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52473-010-052019-10-29C16284748780-1960f7f55-c8f6-8e05-e053-dbdaa90a074aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52473-010-05Odorless Hand Sanitizer Foam150 mL in 1 BOTTLE, PUMPLIQUID1501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52473-010ODORLESS HAND SANITIZER FOAM (BENZALKONIUM CHLORIDE) LIQUID [TINKS]1Legacy NDC, 1 package rows20101005_b9b998fe-37c2-463b-9cba-69795f83ff03.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Benzalkonium ChlorideACTIVE INGREDIENTF5UM2KM3W71
BenzalkoniumACTIVE MOIETY7N6JUD5X6Y1
Aloe Vera LeafINACTIVE INGREDIENTZY81Z83H0X1
Behentrimonium ChlorideINACTIVE INGREDIENTX7GNG3S47T1
Dihydroxyethyl Cocamine OxideINACTIVE INGREDIENT8AR51R3BL51
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDEINACTIVE INGREDIENT0Y0NQR2GH11
Glycereth-2 CocoateINACTIVE INGREDIENTJWM00VS7HC1
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52473-01052473-010-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
Benzalkonium ChlorideF5UM2KM3W7ACTIB
Water059QF0KO0RIACT
Aloe Vera LeafZY81Z83H0XIACT
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE0Y0NQR2GH1IACT
Glycereth-2 CocoateJWM00VS7HCIACT
Behentrimonium ChlorideX7GNG3S47TIACT
Dihydroxyethyl Cocamine Oxide8AR51R3BL5IACT

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
9aaae807-122b-465f-98e8-6f25cfaf74fcb9b998fe-37c2-463b-9cba-69795f83ff032010-08-23WarningsExact identifier
spl id: 9aaae807-122b-465f-98e8-6f25cfaf74fc
spl set id: b9b998fe-37c2-463b-9cba-69795f83ff03

Reported adverse events (FAERS/openFDA)#

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