FDA.reportPublic FDA data

IDLife SANITIZE MOISTURIZING HAND SANITIZER

Manufacturer
Willspeed Technologies LLC
Effective date
2022-01-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:47:03

Label at a glance#

ProductIDLife SANITIZE MOISTURIZING HAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

Kills 99.99 % germs and moisturizes skin.

Dosage and administration

Apply a small amount to hands and rub until dry. Lotion does not replace soap and water.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Kills 99.99 % germs and moisturizes skin.

Warnings

WARNINGS SECTION

For external use only.

Do not use in the eyes.

OTC - DO NOT USE SECTION

In case of eye contact, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or redness develops, or if condition persists more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Instruct children on proper use. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply a small amount to hands and rub until dry. Lotion does not replace soap and water.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Extract, Avena Sativa (Oat) Extract, Behentrimonium Methosulfate, Caprylyl Glycol, Cetearyl Alcohol, Cetrimonium Chloride, Dimethicone, Glycerin, Hydrolyzed Soy Protein, Mentha Piperita (Peppermint) Essential Oil, Phenoxyethanol, Polysorbate 60, Simmondsia Chinensis (Jojoba) Seed Oil, Tetrasodium EDTA, Vitamin A Palmitate, Vitamin E Acetate, Water.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

IDLife

SANITIZE+
MOISTURIZING HAND SANITIZER
Kills 99.9% OF GERMS PROTECTION UP TO 4 HOURS
2 fl. oz. (59mL)

PATENTED FORMULA

IDLife SANITIZE+ MOISTURIZING HAND SANITIZER Kills 99.9% OF GERMS PROTECTION UP TO 4 HOURS 2 fl. oz. (59mL) PATENTED FORMULAIDLife SANITIZE+ MOISTURIZING HAND SANITIZER Kills 99.9% OF GERMS PROTECTION UP TO 4 HOURS 2 fl. oz. (59mL) PATENTED FORMULA

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046442benzalkonium chloride 0.13 % Topical LotionPSN2
1046442benzalkonium chloride 1.3 MG/ML Topical LotionSCD2
1046442benzalkonium chloride 0.13 % Topical LotionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69243-1111-12024-01-30C16284748780-11030e365-0503-111a-e063-dadaa90a10e2IDLife SANITIZE MOISTURIZING HAND SANITIZER
69243-1111-22024-01-30C16284748780-11030e365-0503-111a-e063-dadaa90a10e2IDLife SANITIZE MOISTURIZING HAND SANITIZER
69243-1111-32024-01-30C16284748780-11030e365-0503-111a-e063-dadaa90a10e2IDLife SANITIZE MOISTURIZING HAND SANITIZER
69243-1111-42024-01-30C16284748780-11030e365-0503-111a-e063-dadaa90a10e2IDLife SANITIZE MOISTURIZING HAND SANITIZER
69243-1111-52024-01-30C16284748780-11030e365-0503-111a-e063-dadaa90a10e2IDLife SANITIZE MOISTURIZING HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69243-1111-1IDLife SANITIZE MOISTURIZING HAND SANITIZER30 mL in 1 BOTTLE, PUMPLOTION302
69243-1111-2IDLife SANITIZE MOISTURIZING HAND SANITIZER44 mL in 1 BOTTLE, PUMPLOTION442
69243-1111-3IDLife SANITIZE MOISTURIZING HAND SANITIZER59 mL in 1 BOTTLE, PUMPLOTION592
69243-1111-4IDLife SANITIZE MOISTURIZING HAND SANITIZER118 mL in 1 BOTTLE, PUMPLOTION1182
69243-1111-5IDLife SANITIZE MOISTURIZING HAND SANITIZER237 mL in 1 BOTTLE, PUMPLOTION2372

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69243-1111IDLIFE SANITIZE MOISTURIZING HAND SANITIZER (BENZALKONIUM CHLORIDE) LOTION [WILLSPEED TECHNOLOGIES LLC]2Legacy NDC, 5 package rows20220115_e20dfe84-49a2-4a42-a0ac-995bd3268833.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69243-111169243-1111-1, 69243-1111-2, 69243-1111-3, 69243-1111-4, 69243-1111-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ALOE VERA LEAFZY81Z83H0XIACT
AVENA SATIVA LEAF206PI19V7RIACT
BEHENTRIMONIUM METHOSULFATE5SHP745C61IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
CAPRYLYL GLYCOL00YIU5438UIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
DIMETHICONE92RU3N3Y1OIACT
GLYCERINPDC6A3C0OXIACT
SOY PROTEINR44IWB3RN5IACT
PEPPERMINT OILAV092KU4JHIACT
PHENOXYETHANOLHIE492ZZ3TIACT
VITAMIN A PALMITATE1D1K0N0VVCIACT
JOJOBA OIL724GKU717MIACT
SORBIC ACIDX045WJ989BIACT
EDETATE SODIUMMP1J8420LUIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT

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
ce537db5-479a-4dcb-a3b0-55b53ac26273e20dfe84-49a2-4a42-a0ac-995bd32688332022-01-14WarningsExact identifier
spl id: ce537db5-479a-4dcb-a3b0-55b53ac26273
spl set id: e20dfe84-49a2-4a42-a0ac-995bd3268833

Reported adverse events (FAERS/openFDA)#

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