F4P Hand Sanitizer

Manufacturer
CITY ELECTRIC SUPPLY COMPANY DBA F4P
Effective date
2022-10-14
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:51:01

Label at a glance#

ProductF4P Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Wet hands thoroughly with product and rub until dry without wiping. For children under 6, use only with adult supervision. Not recommended for infants.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Usage

INDICATIONS & USAGE SECTION

To decrease bacteria on skin that could cause disease  Recommended for repeated use

Use anywhere without water

Warnings

WARNINGS SECTION

For external use only-hands


- Flammable. Keep away from heat and flame.
- Discontinue if skin becomes irritated and ask a doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

- Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and rub until dry without wiping.
For children under 6, use only with adult supervision.
Not recommended for infants.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (water), Glycerin, Propylene glycol, Alcohol, Carbomer, Aminomethly Propanol, Parfume

Package Label - 59 mL & 236 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

59 mL label front

59 mL front59 mL front

59 mL labe back

59 mL back59 mL back

Label 236 mL 

236 mL236 mL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN4
1047755ethanol 0.75 ML/ML Topical SolutionSCD4
1047755ethanol 75 % Topical SolutionSY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74970-001-012024-01-30C16284748780-11030e365-6989-111a-e063-dadaa90a10e286885bfb-579e-4fdd-90f0-53c7bbdbb781
74970-001-022024-01-30C16284748780-11030e365-6989-111a-e063-dadaa90a10e286885bfb-579e-4fdd-90f0-53c7bbdbb781

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74970-001-01F4P Hand Sanitizer59 mL in 1 BOTTLE, PLASTICLIQUID594
74970-001-02F4P Hand Sanitizer236 mL in 1 BOTTLE, PLASTICLIQUID2364

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74970-001F4P HAND SANITIZER (ALCOHOL) LIQUID [CITY ELECTRIC SUPPLY COMPANY DBA F4P]4Legacy NDC, 2 package rows20221015_86885bfb-579e-4fdd-90f0-53c7bbdbb781.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74970-00174970-001-01, 74970-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
eb05cbf4-ae44-6068-e053-2a95a90ad1c986885bfb-579e-4fdd-90f0-53c7bbdbb7812022-10-14WarningsExact identifier
spl id: eb05cbf4-ae44-6068-e053-2a95a90ad1c9
spl set id: 86885bfb-579e-4fdd-90f0-53c7bbdbb781

Reported adverse events (FAERS/openFDA)#

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