FDA.reportPublic FDA data

G AND Y ANTIBACTERIAL WET WIPES

Manufacturer
G&Y PRODUCTS INC. | G AND Y PRODUCTS INC. | ERUSLU SAGLIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI
Effective date
2022-02-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:47:54

Label at a glance#

ProductG AND Y ANTIBACTERIAL WET WIPES
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Indications and uses

For handwashing to decrease bacteria on the skin.

Dosage and administration

Storage: Store at room temperature Dispensing: Peel back label slowly. Pull out wipe and reseal label. Close label to retain moisture. Use: Apply wipe thoroughly to hands as desired. Allow to dry without wiping. Disposal: Dispose of used wipes in trash receptable after use. Do not flush.

Storage and handling

Storage: Store at room temperature Dispensing: Peel back label slowly. Pull out wipe and reseal label. Close label to retain moisture. Use: Apply wipe thoroughly to hands as desired. Allow to dry without wiping. Disposal: Dispose of used wipes in trash receptable after use. Do not flush.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13% w/w

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • in the eyes.
  • if you are allergic to any of the ingredients.

When using this product

OTC - WHEN USING SECTION

if eye contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation and redness develop and persist 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

STORAGE AND HANDLING SECTION

  • Storage: Store at room temperature
  • Dispensing: Peel back label slowly. Pull out wipe and reseal label. Close label to retain moisture.
  • Use: Apply wipe thoroughly to hands as desired. Allow to dry without wiping.
  • Disposal: Dispose of used wipes in trash receptable after use. Do not flush.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Benzoic Acid, C12-15 Pareth-12, Dehydroacetic Acid, Fragrance, Glycerin, Phenoxyethanol, Purified Water, Tetrasodium Glutamate Diacetate.

Package label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Kills 99.9% of Germs that may cause illness.

6.3 IN x 7.1 IN

(16 cm x 18 cm)

Questions? +1 (862) 257-3339

You may also report serious side effects to this phone number.

Mon-Fri 9:00 AM - 5:00 PM

Distributed by: G&Y Products, Inc.

25 Shady St, Paterson, NJ 07524

info@gyproduct.com

Country of origin: Turkey

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

G&Y Antibacterial Wet Wipes 20G&Y Antibacterial Wet Wipes 20

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80903-013-202023-07-28C16284748780-1d6a99b39-e8b0-a426-e053-dadaa90af4c2b7bd6f74-b129-3654-e053-2a95a90aa89a
80903-013-202022-02-01C16284748780-1d6a99b39-e8b0-a426-e053-dadaa90af4c2b7bd6f74-b129-3654-e053-2a95a90aa89a
80903-013-202022-01-28C16284748780-1d6a99b39-e8b0-a426-e053-dadaa90af4c2b7bd6f74-b129-3654-e053-2a95a90aa89a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80903-013-20G AND Y ANTIBACTERIAL WET WIPES3.5 mL in 1 PACKAGECLOTH3.53
80903-013-20G AND Y ANTIBACTERIAL WET WIPES20 in 1 PACKAGECLOTH203

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80903-013G AND Y ANTIBACTERIAL WET WIPES CLOTH [G&Y PRODUCTS INC.]3Legacy NDC, 2 package rows20220202_b7bd6f74-b129-3654-e053-2a95a90aa89a.zip

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
80903-01380903-013-20

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
DEHYDROACETIC ACID2KAG279R6RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
C12-15 PARETH-12131316X18LIACT
GLYCERINPDC6A3C0OXIACT
BENZOIC ACID8SKN0B0MIMIACT

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
ff282641-29a5-46d9-ad9f-6c277a91878ab7bd6f74-b129-3654-e053-2a95a90aa89a2022-02-01WarningsExact identifier
spl id: ff282641-29a5-46d9-ad9f-6c277a91878a
spl set id: b7bd6f74-b129-3654-e053-2a95a90aa89a

Reported adverse events (FAERS/openFDA)#

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