YELLOW ESSENTIALS SANITIZING WIPES- 87039-001 cloth

YELLOW ESSENTIALS SANITIZING WIPES by

Drug Labeling and Warnings

YELLOW ESSENTIALS SANITIZING WIPES by is a Otc medication manufactured, distributed, or labeled by Gritt Commercial Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient(s)

Benzalkonium Chloride 0.13% w/w

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

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

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.

KEEP OUT OF REACH OF CHILDREN

· Keep out of reach of children and pets.

DOSAGE & ADMINISTRATION

Directions

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

INACTIVE INGREDIENT

Inactive ingredients

Purified Water, Phenoxyethanol, Ethylhexylglycerin, Propylene Glycol,

Glycerin, Ammonium Chloride, Citric Acid.

PRINCIPAL DISPLAY PANEL

Yellow

ESSENTIALS

SANITIZING

WIPES

2000 WIPES · 8″ × 5″

NDC: 87039-001-01

INGREDIENTS AND APPEARANCE

YELLOW ESSENTIALS SANITIZING WIPES 
87039-001 cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87039-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
AMMONIUM CHLORIDE (UNII: 01Q9PC255D)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CITRIC ACID (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87039-001-01	2000 in 1 BAG	09/01/2025
1		0.001845 g in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	09/01/2025

Labeler - Gritt Commercial Inc. (101913756)