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: FA Hand Sanitizer Liquid 70 100mL

Package Label: FA Hand Sanitizer Liquid 70 200mL

Package Label: FA Hand Sanitizer Liquid 70 500mL

INGREDIENTS AND APPEARANCE

FA HAND SANITIZER LIQUID 70 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74932-310
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	Alcohol	70 mL  in 100 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: 74932-310-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/01/2020
2	NDC: 74932-310-02	200 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/01/2020
3	NDC: 74932-310-03	500 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(74932-310)