X Bright Pro Sanitized Wipes

Manufacturer: PHOENYX DISTRIBUTING., LLC
Effective date: 2024-01-24
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 21:12:41

Label at a glance#

ProductX Bright Pro Sanitized Wipes

Active ingredientALCOHOL

Label structure7 sections

Dosage and administration

wet hands thoroughly with wipe and allow to dry without wiping

Contacts and useful links#

PhoneLabel contact844-901-5005

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Flammable, keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

in the eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop
condition persists for more than 72 hours

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.

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with wipe and allow to dry without wiping

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water

Questions or Comments?

OTC - QUESTIONS SECTION

844-901-5005

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79316-057	X BRIGHT PRO SANITIZED WIPES (ALCOHOL) CLOTH [PHOENYX DISTRIBUTING., LLC]	2	Legacy NDC	20240125_b00129f7-9460-1047-e053-2995a90a65e5.zip

Products#

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

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

X Bright Pro Sanitized Wipes
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79316-057	79316-057-50

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
0fb527c8-e5b1-c8df-e063-6294a90a0652			b00129f7-9460-1047-e053-2995a90a65e5	2024-01-24	Warnings	Exact identifier spl id: 0fb527c8-e5b1-c8df-e063-6294a90a0652 spl set id: b00129f7-9460-1047-e053-2995a90a65e5

Reported adverse events (FAERS/openFDA)#

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