Alexander Hand Sanitizer by Alexander Manufacturing Company Unscented Hand Sanitizer

Alexander Hand Sanitizer by

Drug Labeling and Warnings

Alexander Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Alexander Manufacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ALEXANDER HAND SANITIZER- ethyl alcohol gel 
Alexander Manufacturing Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Unscented Hand Sanitizer

Drug Facts

Active ingredient

Ethyl alcohol 62%

Purpose

Antiseptic

Uses

hand sanitizer to decrease bacteria on the skin 

recommended for repeated use

for use when soap and water are not available.

Warnings

Flammable, keep away from fire/flame.

For external use only

Do not use

in children less than 2 months of age.

on open skin wounds

When using this product do not get into eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if

irritation and redness develop
condition persists for more than 72 hours

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
supervise children under 6 years of age when using this product to avoid swallowing

Other information

store between 15-30° C (59-86° F)

avoid freezing and excessive heat above 40° C (104° F)   

Inactive ingredients carbopol, diisopropylamine, glycerin, water.

Questions? +1-314-842-3344

You may also report serious side effects to this phone number.

Mon- Fri 9:00 AM - 5:00 PM

Antiseptic Hand Sanitizer

Made In USA

ALEXANDER

Packed by: Alexander Manufacturing Company 114 North Linoln Street, Towanda, IL 61776

Packaging

ALEXANDER HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78372-402
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
DIISOPROPYLAMINE (UNII: BR9JLI40NO)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78372-402-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020	07/31/2022
2	NDC: 78372-402-04	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/25/2020	07/31/2022
3	NDC: 78372-402-08	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/01/2020	07/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2020	07/31/2022

Labeler - Alexander Manufacturing Company (062326137)

Revised: 9/2021

Document Id: 0123e220-e8ce-4fea-af28-888e08fb2c3c

34390-5

Set id: bebdd33b-8862-45ec-874e-60c717f51b01

Version: 3

Effective Time: 20210917