USF Inc. Antiseptic Hand Sanitizer

USF Inc. Antiseptic Hand Sanitizer by

Drug Labeling and Warnings

USF Inc. Antiseptic Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by U S Fluids Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

USF INC. ANTISEPTIC HAND SANITIZER- isopropyl alcohol gel 
U S Fluids Inc

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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USF Inc. Antiseptic Hand Sanitizer

Drug Facts

Active ingredient

Isopropyl Alcohol 70% v/v

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

■ Shake well before using ■ 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 (59-83°F)

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

Inactive ingredients

Water, Cellulose Thickener, Glycerin, Hydrogen peroxide

Questions?    1-413-525-0660

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

Mon-Fri 8:00 AM- 4:00 PM

Manufactured for/ Distributed by US Fluids Inc.

202 Benton Drive, East Longmeadow, MA 01028

Packaging

USF INC. ANTISEPTIC HAND SANITIZER 
isopropyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75189-200
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 L  in 100 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75189-200-04	0.12 L in 1 BOTTLE; Type 0: Not a Combination Product	07/28/2020	07/13/2022
2	NDC: 75189-200-06	0.18 L in 1 BOTTLE; Type 0: Not a Combination Product	07/28/2020	07/13/2022
3	NDC: 75189-200-08	0.24 L in 1 BOTTLE; Type 0: Not a Combination Product	07/28/2020	07/13/2022
4	NDC: 75189-200-12	0.35 L in 1 BOTTLE; Type 0: Not a Combination Product	07/28/2020	07/13/2022
5	NDC: 75189-200-16	0.47 L in 1 BOTTLE; Type 0: Not a Combination Product	07/28/2020	07/13/2022
6	NDC: 75189-200-32	0.95 L in 1 BOTTLE; Type 0: Not a Combination Product	07/28/2020	07/13/2022
7	NDC: 75189-200-01	3.80 L in 1 JUG; Type 0: Not a Combination Product	07/28/2020	07/13/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/28/2020	07/13/2022

Labeler - U S Fluids Inc (139405646)

Establishment
Name	Address	ID/FEI	Business Operations
U S Fluids Inc		139405646	manufacture(75189-200)

Revised: 1/2022

Document Id: 2877d8b4-e42e-4f1a-93bd-55625381d81e

34390-5

Set id: aaa89f0e-c328-4bbe-8cd9-64e6d5224d93

Version: 2

Effective Time: 20220106