FDA.reportPublic FDA data

Tiger Wipes

Manufacturer
WHITEHALL PRODUCTS LLC
Effective date
2022-01-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:12:54

Label at a glance#

ProductTiger Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13% Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

avoid contact with the eyes. In case of contact, flush eyes thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develop

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

DOSAGE & ADMINISTRATION SECTION

Locate V notch on side of bag

Tear straight across to open. Do not remove wipes roll from pouch

Pull first wipe from center of roll up through opening of bag

Thread first wipe through dispensing nozzle in lid of floor stand. Please exercise caution with your fingers when pushing wipe through the nozzle.

INDICATIONS & USAGE SECTION

IDEAL FOR: Gyms and Wellness Centers, Schools, Daycare Centers, Restaurants and Nursing Homes.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, n-Alkyl-dimethyl Benzylammonium Chloride, Dmdm Hydantoin, Phenoxyethanol, 2-Bromo-2-Nitropropane-1,3-Dio, Polysorbate 20

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

82536-001-01 800 PCS

Tiger Wipes

Alcohol-Free Formula

Contains Benzalkonium Chloride

IDEAL FOR: Gyms and Wellness Centers, Schools, Daycare Centers, Restaurants and Nursing Homes.

800 Wet Wipes

6" x 8" (15.2cm x 20.3cm)

Pre-Moistened Wipes

Fragrance free

PDPPDP

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
82536-00182536-001-01
79288-020

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
DMDM HYDANTOINBYR0546TOWIACT
N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18)9U1Q4T4ZYSIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
POLYSORBATE 207T1F30V5YHIACT
PHENOXYETHANOLHIE492ZZ3TIACT
BRONOPOL6PU1E16C9WIACT

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
de0055bb-a0bc-62aa-e053-2995a90a1197d610a334-3c49-067d-e053-2995a90a2a482022-05-01WarningsExact identifier
spl set id: d610a334-3c49-067d-e053-2995a90a2a48

Reported adverse events (FAERS/openFDA)#

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