FDA.reportPublic FDA data

YNOT

Manufacturer
Y-Not design and manufacturing inc.
Effective date
2022-11-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:46:34

Label at a glance#

ProductYNOT
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

 For sanitizing to help reduce bacteria on the skin.

Dosage and administration

Gently pull back resealable label,remove and use wipe required. Reseal back after use to avoid evaporation of alcohol.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

Do not use

  • In or near the eyes
  • On open skin wounds or burns.

When using this product

  • Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if Irritation or rash occurs. These may be signs of a serious condition.

Uses

INDICATIONS & USAGE SECTION

 For sanitizing to help reduce bacteria on the skin.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Gently pull back resealable label,remove and use wipe required.
  • Reseal back after use to avoid evaporation of alcohol.

Other Information

SPL UNCLASSIFIED SECTION

  • This product is insoluble in water, dispose of used wipes in trash.
  • Do not flush into toilet.
  • This product may discolour certain fabrics or surfaces.

keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Unless under adult supervision.
  • If swallowed, medical get help or contact a Poison Control Center right away.

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Alkyl polyglucoside, Aqua, Benzalkonium chloride, C12-14 Alkyl dimethyl ethylbenzyl ammonium chloride, Cetylpyridinium Chloride, Chlorphenesin, Disodium EDTA, Glycerin, Propylene glycol.

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

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
75720-00375720-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
APG-1387E53VN70K2XIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14)G258TFN61XIACT
CETYLPYRIDINIUM CHLORIDED9OM4SK49PIACT
CHLORPHENESINI670DAL4SZIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALCOHOL3K9958V90MACTIB

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
101631c5-890e-b9dd-e063-6294a90a5832fd8d1237-6d26-43eb-9528-577005cb91c52024-01-29WarningsExact identifier
spl set id: fd8d1237-6d26-43eb-9528-577005cb91c5

Reported adverse events (FAERS/openFDA)#

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