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 Ingredient

Ethyl Alcohol 62%

Purpose

Antispetic

Uses

To decrease bacteria on the skin that could cause disease

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. D 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-Principle Display Panel

INGREDIENTS AND APPEARANCE

SEA AND SKI ADVANCE HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73440-3131
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	1171.73 g  in 1889.89 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	540.6 g  in 1889.89 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73440-3131-2	3.785 g in 1 BOTTLE; Type 0: Not a Combination Product	04/30/2020
2	NDC: 73440-3131-1	3.785 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/30/2020

Labeler - Cross-Brands Contract Filling (116950257)

Establishment
Name	Address	ID/FEI	Business Operations
Cross-Brands Contract Filling		116950257	manufacture(73440-3131) , label(73440-3131) , pack(73440-3131)