Fast Orange_Permatex 370.001/370AE rev 1 Advanced Hand Sanitizer

Antibacterial Hand Sanitizer by

Drug Labeling and Warnings

Antibacterial Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by PERMATEX, Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ANTIBACTERIAL HAND SANITIZER- alcohol gel 
PERMATEX

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Fast Orange_Permatex 370.001/370AE rev 1
Advanced Hand Sanitizer

Active Ingredient

Ethyl alcohol 70%

purpose

Antiseptic

Use

• to decrease bacteria on the skin that could cause disease
• recommended for repeated use

Warnings

For external use only: hands

Flammable

Keep away from heat and flame

When using this product

• keep out of eyes. In case of contact with eyes, flush thoroughly with water.
• avoid contact with broken skin
• do not inhale or ingest

Stop use and ask a doctor if

• irritation or redness develops
• 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 thoroghly with product and allow to dry without wiping
• for children under 6, use only under adult supervision
• not recommended for infants

Other information

• do not store above 105⁰ F
• may discolor some fabrics
• harmful to wood finishes and plastics

Inactive ingredients

water, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4

*Effective at eliminating more than 99.99% of many common harmful germs and bacteria in as little as 15 seconds

PERMATEX and design are TMs of Illinois Tool Works, Inc. 2016 Permatex, a division of ITW.

Solon, OH 44139/ Assembled in U.S.A. with U.S. and global materials

www.permatex.com

Principal display panel

Fast Orange

Moisturizing Formula

Advanced Hand Sanitizer

Kills more than 99.99% of germs

Moisturizing formula with Vitamin E

8 FL OZ (236 mL)

ANTIBACTERIAL HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70616-370
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)
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
SULISOBENZONE (UNII: 1W6L629B4K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70616-370-16	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/02/2015	01/26/2022
2	NDC: 70616-370-34	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/02/2015	01/26/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	02/02/2015	01/26/2022

Labeler - PERMATEX (964477025)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(70616-370)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(70616-370)

Revised: 10/2024

Document Id: 252770f2-36eb-8ae4-e063-6294a90aae06

34390-5

Set id: dc6eb382-7b25-4e24-8087-a6d9c32c63ae

Version: 5

Effective Time: 20241023