Summit 375 Gel Alcohol Hand Sanitizer - R.L. Williams Company

Manufacturer: R.L. Williams Company
Effective date: 2026-04-29
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:55:22

Label at a glance#

ProductSummit 375 Gel Alcohol Hand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

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

Dosage and administration

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.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Skin Sanitizer

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

OTHER SAFETY INFORMATION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product Label - 850 mL Cartridge (Front)

Product Label - 850 mL Cartridge (Back)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0810080570016	GTIN-13: 0810080570016 EAN-13: 0810080570016 GTIN-12: 810080570016 UPC-A: 810080570016 GTIN storage (14 digits): 00810080570016	Summit375_Back.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
23590-400-10	Summit 375 Gel Alcohol Hand Sanitizer	850 mL in 1 BOTTLE, PUMP	GEL	850		1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Summit 375 Gel Alcohol Hand Sanitizer
Alcohol
DIISOPROPYLAMINE
GLYCERIN
PROPYLENE GLYCOL
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
23590-400	23590-400-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
DIISOPROPYLAMINE	BR9JLI40NO	IACT
ALCOHOL	3K9958V90M	ACTIB
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
WATER	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Summit 375 Gel Alcohol Hand Sanitizer	ALCOHOL	R.L. Williams Company	509cc442-09f8-d17f-e063-6394a90a77ea	2026-04-29	Warnings	Exact identifier ndc (package): 23590-400-10 ndc (product): 23590-400 ndc11 (package): 23590040010 spl id: 509cd5d6-2791-73d1-e063-6294a90addda spl set id: 509cc442-09f8-d17f-e063-6394a90a77ea

Reported adverse events (FAERS/openFDA)#

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