FDA.reportPublic FDA data

Ynot Hand Hand Sanitizer

Manufacturer
Y-NOT DESIGN & MFG. INC
Effective date
2020-04-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:34:35

Label at a glance#

ProductYnot Hand Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

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

Do not use 

  • In children less than 2 months of age
  • On open skin wounds

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf, Extract, Carbomer, Glycerin, Parfum(Fragrance), Propylene Glycol,Sodium Hydroxide, Water(Aqua).

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label 100 mL

100 mL100 mL

Label 500 mL

500 mL500 mL

Label 1000 mL

1000 mL1000 mL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75720-002-012024-01-30C16284748780-1e4f33bdf-a3b8-d8a0-e053-dadaa90a6e4e08095efb-78b2-4ff7-ae65-7b8d3f6ba6f4
75720-002-022024-01-30C16284748780-1e4f33bdf-a3b8-d8a0-e053-dadaa90a6e4e08095efb-78b2-4ff7-ae65-7b8d3f6ba6f4
75720-002-032024-01-30C16284748780-1e4f33bdf-a3b8-d8a0-e053-dadaa90a6e4e08095efb-78b2-4ff7-ae65-7b8d3f6ba6f4
75720-002-012022-07-29C16284748780-1e4f33bdf-a3b8-d8a0-e053-dadaa90a6e4e08095efb-78b2-4ff7-ae65-7b8d3f6ba6f4
75720-002-022022-07-29C16284748780-1e4f33bdf-a3b8-d8a0-e053-dadaa90a6e4e08095efb-78b2-4ff7-ae65-7b8d3f6ba6f4
75720-002-032022-07-29C16284748780-1e4f33bdf-a3b8-d8a0-e053-dadaa90a6e4e08095efb-78b2-4ff7-ae65-7b8d3f6ba6f4

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75720-00275720-002-01, 75720-002-02, 75720-002-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
SODIUM HYDROXIDE55X04QC32IIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALOE VERA LEAFZY81Z83H0XIACT

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
10161615-0be7-a7f8-e063-6294a90a130208095efb-78b2-4ff7-ae65-7b8d3f6ba6f42024-01-29WarningsExact identifier
spl set id: 08095efb-78b2-4ff7-ae65-7b8d3f6ba6f4

Reported adverse events (FAERS/openFDA)#

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