FA HAND SANITIZER LIQUID 70- alcohol spray

FA Hand Sanitizer Liquid 70 by

Drug Labeling and Warnings

FA Hand Sanitizer Liquid 70 by is a Otc medication manufactured, distributed, or labeled by FA Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: Ethyl Alcohol 70% w/w

INACTIVE INGREDIENT

Inactive ingredients:

Water, Glycerin

PURPOSE

PURPOSE: Antiseptic

WARNINGS

Warnings:

For external use only. Flammable. Keep away from heat or flame
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When using this product ■ do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water ■ avoid contact with broken skin ■ do not inhale or ingest
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Stop use and ask a doctor if irritation or rash appears and lasts

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.

Uses

Uses

■ Hand sanitizer to help reduce bacteria that potentially can cause disease.

Directions

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

Other Information

■ Store below 86℉(Between 1~30℃)
■ May discolor certain fabrics or surfaces

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FA HAND SANITIZER LIQUID 70 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74932-300
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	Alcohol	42 mL  in 60 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74932-300-01	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/01/2020

Labeler - FA Inc. (557816103)

Registrant - FA Inc. (557816103)

Establishment
Name	Address	ID/FEI	Business Operations
FA Inc.		557816103	manufacture(74932-300)