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 Ingredients

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 ingredients.

When using this product

OTC - WHEN USING SECTION

if eye contact occurs, rinse eyes thoroughly with water

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.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

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,

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 90G&Y Antibacterial Wet Wipes 90

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
80903-013-902023-07-28C16284748780-1d6a99b39-e84a-a426-e053-dadaa90af4c2b7b0e822-ecc7-401e-e053-2a95a90ad7f4
80903-013-902022-02-01C16284748780-1d6a99b39-e84a-a426-e053-dadaa90af4c2b7b0e822-ecc7-401e-e053-2a95a90ad7f4
80903-013-902022-01-28C16284748780-1d6a99b39-e84a-a426-e053-dadaa90af4c2b7b0e822-ecc7-401e-e053-2a95a90ad7f4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80903-013-90G AND Y ANTIBACTERIAL WET WIPES3.5 mL in 1 PACKAGECLOTH3.53
80903-013-90G AND Y ANTIBACTERIAL WET WIPES90 in 1 PACKAGECLOTH903

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_b7b0e822-ecc7-401e-e053-2a95a90ad7f4.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
80903-01380903-013-90

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
WATER059QF0KO0RIACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
DEHYDROACETIC ACID2KAG279R6RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
PHENOXYETHANOLHIE492ZZ3TIACT
C12-15 PARETH-12131316X18LIACT
BENZOIC ACID8SKN0B0MIMIACT
GLYCERINPDC6A3C0OXIACT

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
3df9da9a-9036-4803-8dee-c867eb0f6255b7b0e822-ecc7-401e-e053-2a95a90ad7f42022-02-01WarningsExact identifier
spl id: 3df9da9a-9036-4803-8dee-c867eb0f6255
spl set id: b7b0e822-ecc7-401e-e053-2a95a90ad7f4

Reported adverse events (FAERS/openFDA)#

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