YNOT HAND HAND SANITIZER- alcohol gel

Ynot Hand Hand Sanitizer by

Drug Labeling and Warnings

Ynot Hand Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Y-NOT DESIGN & MFG. INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Alcohol 75%

Purpose

Antiseptic

Uses

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

Warnings

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.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

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

Directions

• 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

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

Inactive ingredients

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

Package Label - Principal Display Panel

Label 100 mL

Label 500 mL

Label 1000 mL

INGREDIENTS AND APPEARANCE

YNOT HAND HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75720-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75720-002-01	100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/21/2020
2	NDC: 75720-002-02	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/21/2020
3	NDC: 75720-002-03	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/21/2020

Labeler - Y-NOT DESIGN & MFG. INC (620485735)