FIRST Safety INSTANT SANITIZER WIPES

First Safety by

Drug Labeling and Warnings

First Safety by is a Otc medication manufactured, distributed, or labeled by General Printing & Design, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

FIRST SAFETY- alcohol cloth 
General Printing & Design, 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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FIRST Safety INSTANT SANITIZER WIPES

Drug Facts

Active ingredient

Alcohol 75% by volume

Purpose

Antiseptic

Uses  For hand washing to decrease bacteria on the skin. Apply topically to the skin to help prevent cross contamination. Recommended for repeated use. Dries in seconds when used as directed.

Warnings Flammable, keep away from fire or flame. For external use only. When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions Use wipe to thoroughly wipe hands, fingers, and wrists. Be sure to use the entire wipe. Allow to dry. For dirty hands, use first wipe to clean hands, then discard wipe; sanitize with second wipe. Discard after single use - Do not flush.

Inactive ingredients Water, Glycerin, Vitamin E

Moisturizing formula with Vitamin E leaves hands feeling soft

75% Alcohol

Fast & Effective

Moisturizing Formula

Kills 99.9% of Germs

DISTRIBUTED BY:

FIRST Safety

45 BARTLETT STREET

MARLBOROUGH, MA 01752

www.firstsafetyco.com

800-258-2000

MADE IN CHINA

Packaging

FIRST SAFETY 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76720-013
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76720-013-01	20 in 1 BAG	07/29/2020	07/29/2022
1		5.29 mL in 1 PACKAGE; Type 0: Not a Combination Product
2	NDC: 76720-013-02	72 in 1 CANISTER	07/29/2020	07/29/2022
2		5.29 mL in 1 PACKAGE; Type 0: Not a Combination Product
3	NDC: 76720-013-03	80 in 1 BAG	07/29/2020	07/29/2022
3		5.29 mL in 1 PACKAGE; Type 0: Not a Combination Product
4	NDC: 76720-013-04	100 in 1 CANISTER	07/29/2020	07/29/2022
4		5.29 mL in 1 PACKAGE; Type 0: Not a Combination Product
5	NDC: 76720-013-05	700 in 1 CANISTER	07/29/2020	07/29/2022
5		5.29 mL in 1 PACKAGE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/29/2020	07/29/2022

Labeler - General Printing & Design, Inc. (066630757)

Revised: 7/2022

Document Id: 053837bf-1c4f-4a5d-813c-22738af7fa73

34390-5

Set id: d8627311-18a4-40a6-80a0-81e9e40eb4c4

Version: 4

Effective Time: 20220713