HAND SANITIZER- isopropyl alcohol gel

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Maryland Correctional Enterprises. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients:

Isopropyl Alcohol >/= 70.1%

INACTIVE INGREDIENT

Inactive Ingredients:
Water, Betaine Anhydrous, Anionic Water Soluble Polymer,
Amino Methyl Propanol, DL Alpha Tocopherol Acetate

WARNINGS

For external use only. Flammable. Keep away from heat or flame

PURPOSE

Use[s] Hand sanitizer to help reduce bacteria that potentially
can cause disease.

DO NOT USE

Do not use
in children less than 2 months of age
on open skin wounds

INDICATIONS & USAGE

For use when soap and water are not
available.

WHEN USING

When using this product keep out of eyes, ears, and mouth. In
case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

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

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

DOSAGE & ADMINISTRATION

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

STORAGE AND HANDLING

Other information
Store between 59-86F (15-30C)
Avoid freezing and excessive heat above 140F (40C)

PRINCIPAL DISPLAY PANEL

​94 mL NDC: 74689-000-94

PRINCIPAL DISPLAY PANEL

47 mL NDC: 74689-000-47

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
isopropyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74689-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70.1 mL  in 70.1 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
BETAINE (UNII: 3SCV180C9W)
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74689-000-94	94 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/03/2020
2	NDC: 74689-000-47	47 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/03/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/03/2020

Labeler - Maryland Correctional Enterprises (021961458)

Establishment
Name	Address	ID/FEI	Business Operations
Maryland Correctional Enterprises		021961458	manufacture(74689-000)