ANTIMICROBIAL ALCOHOL HAND- alcohol patch

Antimicrobial Alcohol Hand by

Drug Labeling and Warnings

Antimicrobial Alcohol Hand by is a Otc medication manufactured, distributed, or labeled by Geri-Gentle Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Alcohol 65.9% by volume

Purpose

Antiseptic  

Uses

• Antiseptic 
• For handwashing to decrease bacteria on the skin, assisting ill persons, and before contact with a person under medical care or treatment
• Apply topically to the skin to help prevent cross-contamination
• Recommended for repeated use 
• Dries in seconds

Warnings

• Flammable, keep away from fire or flame
• For external use only

Do not use

• in or make contact with the eyes
• Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a physician 

Keep this our of reach of children

• unless under adult supervision 
• If swallowed, get medical help or contact a Poison Center immediately

Directions

• To start feed: Remove cover and discard seal from container. From center of toweled roll, pull up wipe corner, tear off fist wipe for use. Twist next wipe into a point and thread through the hole in the container cover. Pull through about one inch. Replace cover. Pull out wipes as needed and snap off at 90° angle. Keep cap closed to prevent moisture loss
• Wipe hands , fingers, interdigital areas and wrists thoroughly with towelette. Be sure to utilize the entire wipe surface. Allow to dry
• If hands are visibly soiled or contaminated, use first wipe to clean hands, then discard wipe, Sanitize with a second wipe
• Discard after single use

Other information

Lot No. and Expiration Date can be found on canister

Inactive ingredients

Water, Propylene Glycol, Glycerin, Carbomer, Triethanolamine, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Tetrasodium EDTA

SPL UNCLASSIFIED SECTION

Package Labeling:

INGREDIENTS AND APPEARANCE

ANTIMICROBIAL ALCOHOL HAND 
alcohol patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69771-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65.9 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
EDETATE SODIUM (UNII: MP1J8420LU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69771-002-00	135 in 1 CANISTER	04/05/2017
1		6.59 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/05/2017

Labeler - Geri-Gentle Corporation (080367686)