FDA.reportPublic FDA data

YELLOW ESSENTIALS SANITIZING WIPES

Manufacturer
Gritt Commercial Inc.
Effective date
2025-12-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:28:38

Label at a glance#

ProductYELLOW ESSENTIALS SANITIZING WIPES
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient(s)

Benzalkonium Chloride 0.13% w/w

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Use(s)

For hand sanitizing to decrease bacteria on the skin.

Recommended for repeated use.

Specially designed for the following occasions:

· Gym and Fitness Centers.

· Beauty Centers and Massage Therapy Spas.

· Yoga & Dance Studios.

WARNINGS SECTION

Warnings

· Keep out of reach of children and pets.

· Dispose of product thoroughly.

· Do not flush down the toilet.

· Keep away from eyes. In case of contact with eyes,

rinse immediately with plenty of water for several minutes.

· Do not ingest. In case of ingestion, do not induce vomiting and

consult a doctor immediately.

· If you have hypersensitivity to any ingredient, do not use the

product.

· Stop usage if skin irritation occurs and consult a doctor; keep wipes

in original packaging.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

· Keep out of reach of children and pets.

DOSAGE & ADMINISTRATION SECTION

Directions

Wet targeted area thoroughly with product and let dry without wiping.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Purified Water, Phenoxyethanol, Ethylhexylglycerin, Propylene Glycol,

Glycerin, Ammonium Chloride, Citric Acid.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Yellow

ESSENTIALS

SANITIZING

WIPES

2000 WIPES · 8″ × 5″

NDC: 87039-001-01

Product LabelProduct Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN2
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD2
1038558benzalkonium chloride 0.13 % Topical ClothSY2
1038558benzalkonium chloride 0.13 % Topical SwabSY2
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY2
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY2
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130810162792862GTIN-13: 0810162792862
EAN-13: 0810162792862
GTIN-12: 810162792862
UPC-A: 810162792862
GTIN storage (14 digits): 00810162792862		Product Label.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87039-001-01YELLOW ESSENTIALS SANITIZING WIPES2000 in 1 BAGCLOTH20002
87039-001-01YELLOW ESSENTIALS SANITIZING WIPES0.001845 g in 1 PATCHCLOTH0.0018452

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87039-00187039-001-01

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
AMMONIUM CHLORIDE01Q9PC255DIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
CITRIC ACID2968PHW8QPIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT

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
YELLOW ESSENTIALS SANITIZING WIPES87039-001Gritt Commercial Inc.3d403feb-0d15-d6cd-e063-6394a90a15e62025-12-25WarningsExact identifier
ndc (package): 87039-001-01
ndc (product): 87039-001
ndc11 (package): 87039000101
spl id: 46c2be65-739d-0488-e063-6294a90a291d
spl set id: 3d403feb-0d15-d6cd-e063-6394a90a15e6

Reported adverse events (FAERS/openFDA)#

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