SUMMIT 375 GEL ALCOHOL HAND SANITIZER- alcohol gel

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Skin Sanitizer

Uses

• Hand sanitizer to help reduce bacteria on the skin
• Recommended for repeated use

Warnings

Flammable, keep away from fire or flame.

For external use only.

When using this product do not use around or near the eyes. If contact occurs, flush eyes with water and contact a doctor immediately.

Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Dispense an adequate amount in your palm to cover all surface of hands completely.
• Rub hands together until dry.
• Supervise children in the use of this product.

Other Information

• Do not store above 100 ºF (38 ºC)
• May discolor some fabrics

Inactive Ingredients

Water, Glycerin, Carbomer, Propylene Glycol, Diisopropylamine, Fragrance

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SUMMIT 375 GEL ALCOHOL HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 23590-400
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
DIISOPROPYLAMINE (UNII: BR9JLI40NO)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	white (water white - colorless, crystal clear)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 23590-400-10	850 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/29/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/29/2026

Labeler - R.L. Williams Company (099976362)