SEA AND SKI ADVANCE HAND SANITIZER- ethyl alcohol gel

Sea and Ski Advance Hand Sanitizer by

Drug Labeling and Warnings

Sea and Ski Advance Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Cross-Brands Contract Filling, Cross Brands Contract Filling. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Alcohol 62%

Purpose

Antiseptic

Uses

Uses to decrease bacteria on the skin that could cause diesease

recommended for repeated use

Warnings

For external use only: Hands

Flammable, keep away from fire or flame

When using

When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest

Stop use

Stop Use and ask a doctor if irritation or redness develops condition persists for more than 72 hours.

Keep out of reach of children

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

Directions

wet hands thoroughly with product and allow to dry without wiping for children under 6, use only under adult supervision not recommended for infants

Other information

do not store above 105°F may discolor some fabrics harmful to wood finishes and plastics

Inactive Ingredients

acrylates copolymer*, aloe barbadensis leaf extract carbomer*, tocopheryl acetate (vitamin E), triethanolamine, water

*contains one or more of these ingredients

Package Label Princial Display Panel

Sea & Ski Ultra Light Dri-Gel Hand Sanitizer Moisturizing Aloe Alcohol Antispetic Helps Reduce Bacteria 2.4FL OZ (71 mL)

INGREDIENTS AND APPEARANCE

SEA AND SKI ADVANCE HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73440-2135
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	146.94 mL  in 237 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	white (Clear)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73440-2135-1	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/01/2020

Labeler - Cross-Brands Contract Filling (117871824)

Establishment
Name	Address	ID/FEI	Business Operations
Cross Brands Contract Filling		117871824	manufacture(73440-2135) , label(73440-2135) , pack(73440-2135)