HAND SPRITZER- ethyl alcohol gel

Hand Spritzer by

Drug Labeling and Warnings

Hand Spritzer by is a Otc medication manufactured, distributed, or labeled by Hand Spritzer Llc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient(s)

Ethyl alcohol 80% v/v

Purpose

Antiseptic

Use(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 Center 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 (59-86F)
Avoid freezing and excessive heat above 40C (104F)

INACTIVE INGREDIENT

Inactive ingredients RODI water, hydrogen peroxide, glycerin, methocellulose, carbopol, aloe

SPL UNCLASSIFIED SECTION

Ethyl Alcohol Antiseptic

80% Topical Solution

Hand Sanitizer

Non-sterile Solution

Packaging

INGREDIENTS AND APPEARANCE

HAND SPRITZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77276-428
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLCELLULOSE, UNSPECIFIED (UNII: Z944H5SN0H)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ALOE (UNII: V5VD430YW9)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77276-428-08	235 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/23/2020
2	NDC: 77276-428-16	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/23/2020

Labeler - Hand Spritzer Llc (130846471)