Patterson Dental Antimicrobial Gel

Patterson Antimicrobial Gel Hand Sanitizer by

Drug Labeling and Warnings

Patterson Antimicrobial Gel Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Patterson Dental. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PATTERSON ANTIMICROBIAL GEL HAND SANITIZER- alcohol gel 
Patterson Dental

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.

----------

Patterson Dental Antimicrobial Gel

Drug Facts

Active Ingredient:

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Uses: To decrease bacteria on the skin that potentially can cause disease. Recommended for repeated use.

Warnings:

Flammable, keep away from heat or flame. For external use only.

Keep out of eyes, ears or mouth. In case of eye contact, flush with water.

Stop use and ask a doctor if irritation and redness develop or if condition persists more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Children should be supervised by an adult when using this product.

Directions: Apply sufficient amount of product to your palm to cover both hands. Rub until dry.

Other Information: May discolor certain fabrics and surfaces.

Inactive ingredients: Acrylates/C 10/30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, FD&C Blue 1, FD&C Yellow 5, Fragrance, Isopropyl Alcohol, PEG/PPG-18/18 Dimethicone, Triethanolamine, Vitamin E, Water

Manufactured for:

Patterson Dental Supply, Inc.

1031 Mendota Heights Road

St. Paul, MN 55120

PATTERSON DENTAL

Patterson® Waterless Antimicrobial Gel

SPECIALLY DEVELOPED FOR HEALTHCARE PROFESSIONALS

Enriched with Aloe Vera and Vitamin E to moisturize skin, prevent dryness and reduce loss of moisture.

Free from petroleum products.

For external use only.

18 fl oz (532 mL)

PATTERSON ANTIMICROBIAL GEL HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50227-3000
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
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 132584PQMO)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
TROLAMINE (UNII: 9O3K93S3TK)
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50227-3000-2	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/27/2021	03/18/2023
2	NDC: 50227-3000-3	532 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/27/2021	03/23/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/27/2021	03/23/2023

Labeler - Patterson Dental (171843584)

Revised: 1/2023

Document Id: f27988e1-47f3-be4c-e053-2a95a90ab398

34390-5

Set id: b9e85efe-5b3c-8497-e053-2995a90a98a5

Version: 2

Effective Time: 20230102