SURFSIDE INN AND SUITES UNIVERSAL ORLANDO HAND SANITIZER GEL- ethyl alcohol gel

Surfside Inn and Suites Universal Orlando Hand Sanitizer Gel by

Drug Labeling and Warnings

Surfside Inn and Suites Universal Orlando Hand Sanitizer Gel by is a Otc medication manufactured, distributed, or labeled by Carretta USA, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Ethyl Alcohol 75% v/v

Purpose

Antiseptic

Uses[s]

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.

If swallowed, get medical help or contact a Poison Control 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 (59-83F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive Ingredients:

Water,Glycerin,Propylene glycol,Carbomer,Aloe Vera Extract,Triethanolamine,Disodium Edta

SPL UNCLASSIFIED SECTION

*99.99% of most common germs.

Distributed by:Carretta USA, Inc.

1500 County Road 517, Ste. 210

Hackettstown, NJ 07840

Packaging

INGREDIENTS AND APPEARANCE

SURFSIDE INN AND SUITES UNIVERSAL ORLANDO HAND SANITIZER GEL 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78828-115
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TROLAMINE (UNII: 9O3K93S3TK)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78828-115-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/12/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/12/2020

Labeler - Carretta USA, Inc (010851173)