FDA.reportPublic FDA data

Antibacterial Wet Wipe

Manufacturer
Innovation Specialties
Effective date
2020-04-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:35:44

Label at a glance#

ProductAntibacterial Wet Wipe
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

Open packet, remove and unfold pre-moistened tissue. Wipe hands including nails and cuticles. Allow to dry without wiping. Discard properly after use.

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose:

OTC - PURPOSE SECTION

Antiseptic

Use:

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin.

Warnings

WARNINGS SECTION

FOR EXTERNAL USE ONLY.

Keep away from eyes. In case of eye contact, flush thoroughly with water and then seek medical advice.

Discontinue use if irritation and redness develops.

Do not flush down toilet.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Directions

DOSAGE & ADMINISTRATION SECTION

Open packet, remove and unfold pre-moistened tissue. Wipe hands including nails and cuticles. Allow to dry without wiping. Discard properly after use.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua, Glycerin, Phenoxyethanol, Benzoic Acid, Polysorbate 20, Aloe Barbadensis Leaf Juice, Sodium Citrate

Questions? HOTLINE # 1-855-755 5346

OTC - QUESTIONS SECTION

NPN# 80062390

Made in China For Innovation Line Culver City,

CA 90230

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AntibacAntibac

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76138-12376138-123-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PHENOXYETHANOLHIE492ZZ3TIACT
BENZOIC ACID 2-(2,4,6-TRICHLOROPHENYL)HYDRAZIDEV78NIQ357KIACT
POLYSORBATE 207T1F30V5YHIACT
ALOE VERA LEAFZY81Z83H0XIACT
SODIUM CITRATE1Q73Q2JULRIACT

Source Document#

Source XML · Source PDF

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
3780b85f-8823-4232-9748-9700dac2a90ece0a36f5-ef14-49cb-9be2-8df153cbd4fe2022-12-05WarningsExact identifier
spl set id: ce0a36f5-ef14-49cb-9be2-8df153cbd4fe

Reported adverse events (FAERS/openFDA)#

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