FlashWipes

Manufacturer
Urban Attitudes Holdings Ltd
Effective date
2020-09-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:16:09

Label at a glance#

ProductFlashWipes Lavender Bliss
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Storage and handling

Other information store between 15-30°C (59-86°F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Benzalkonium Chloride 0.1%

OTC - PURPOSE SECTION

Purpose
Antiseptic

INDICATIONS & USAGE SECTION

Uses

  • to decrease bacteria on the skin
  • recommended for repeated use

WARNINGS SECTION

Warnings

For external use only

OTC - WHEN USING SECTION

When using this product keep away from eyes. In case of eye contact, rinse eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION SECTION

Directions

rub wipe thoroughly over all sufaces of both hands and allow to dry.

STORAGE AND HANDLING SECTION

Other information

store between 15-30°C (59-86°F)

INACTIVE INGREDIENT SECTION

Inactive ingredients

water, glycerin, methylchloroisothiazolinone, methylisothiazonlinone, PEG-40 hydrogenated castor oil, tetrasodium EDTA, fragrance

SPL UNCLASSIFIED SECTION

MADE IN PERU

FLASH WIPES IS DISTRIBUTED BY AND IS A REGISTERED TRADEMARK OF

URBAN ATTITUDES HOLDINGS LTD.

GREAT NECK, NY 11023(516) 206-3672

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ANTISEPTIC HAND SANITIZER

FLASHWIPES

LAVENDER BLISS

GENTLE ON HANDS TOUGH ON DIRT

KILLS UP TO 99.99% OF GERMS

BENZALKONIUM CHLORIDE 0.1%

30 SHEETS WET WIPES

(2 ROLLS OF 15 REFILLABLE WIPES.)

6.5 IN. x 6 IN. (15.2 CM x 16.5 CM)

canister Lav Blisscanister Lav Bliss

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
77185-00577185-005-30, 77185-005-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
af87b0e8-40d9-1ef7-e053-2995a90ac444ae7f5091-7d99-8da7-e053-2995a90acf3c2020-09-17WarningsExact identifier
spl set id: ae7f5091-7d99-8da7-e053-2995a90acf3c

Reported adverse events (FAERS/openFDA)#

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