FDA.reportPublic FDA data

Freshorize

Manufacturer
FRESHORIZE, LTD.
Effective date
2020-05-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:14:06

Label at a glance#

ProductFreshorize
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

For handwashing to decrease bacteria on the skin - recommended for repeated use

Dosage and administration

Tear open packet, unfold and use wipe on surface or hands. Allow to air dry without washing Supervise children under 6 years in the use of this product

Label contents#

Full prescribing information#

Active lngredient  

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70 %v/v

Purpose

OTC - PURPOSE SECTION

Hand wipes

Uses

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin - recommended for repeated use

Warnings  

WARNINGS SECTION


For external use only.

Flammable. Keep away from fire or flame.

Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

Keep out of reach of children.

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

Directions

DOSAGE & ADMINISTRATION SECTION

Tear open packet, unfold and use wipe on surface or hands.

Allow to air dry without washing

Supervise children under 6 years in the use of this product

Inactives 

INACTIVE INGREDIENT SECTION

Water (Aqua)

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.

Other information

SPL UNCLASSIFIED SECTION

  • Store at 20°C to 25°C (68° to 77°F)
  • May discolor certain fabrics.

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1489307ethanol 70 % Medicated PadPSN1
1489307ethanol 0.7 ML/ML Medicated PadSCD1
1489307ethanol 70 % Medicated PadSY1
1489307ethanol 70 % Medicated WipesSY1
1489307ethyl alcohol 70 % ClothSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52305-500-102022-01-28C16284748780-1d6a99b39-d9b0-a426-e053-dadaa90af4c2Sanitizing Wipe
52305-500-202022-01-28C16284748780-1d6a99b39-d9b0-a426-e053-dadaa90af4c2Sanitizing Wipe
52305-500-302022-01-28C16284748780-1d6a99b39-d9b0-a426-e053-dadaa90af4c2Sanitizing Wipe
52305-500-402022-01-28C16284748780-1d6a99b39-d9b0-a426-e053-dadaa90af4c2Sanitizing Wipe
52305-500-502022-01-28C16284748780-1d6a99b39-d9b0-a426-e053-dadaa90af4c2Sanitizing Wipe

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52305-500-10Freshorize1.4 mL in 1 PACKETCLOTH1.41
52305-500-10Freshorize1 in 1 PACKETCLOTH11
52305-500-20Freshorize14 mL in 1 PACKETCLOTH141
52305-500-20Freshorize10 in 1 PACKETCLOTH101
52305-500-30Freshorize35 mL in 1 PACKETCLOTH351
52305-500-30Freshorize25 in 1 PACKETCLOTH251
52305-500-40Freshorize50 in 1 PACKETCLOTH501
52305-500-40Freshorize70 mL in 1 PACKETCLOTH701
52305-500-50Freshorize100 in 1 PACKETCLOTH1001
52305-500-50Freshorize140 mL in 1 PACKETCLOTH1401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52305-500FRESHORIZE (ALCOHOL) CLOTH [FRESHORIZE, LTD.]1Legacy NDC, 10 package rows20200521_f03f86e8-3052-41c9-9070-6b9a67ca7283.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52305-50052305-500-10, 52305-500-20, 52305-500-30, 52305-500-40, 52305-500-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
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
db20b959-a0c6-41d8-b473-7a302d57ac4cf03f86e8-3052-41c9-9070-6b9a67ca72832020-05-16WarningsExact identifier
spl id: db20b959-a0c6-41d8-b473-7a302d57ac4c
spl set id: f03f86e8-3052-41c9-9070-6b9a67ca7283

Reported adverse events (FAERS/openFDA)#

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