MY MEDIC HAND SANITIZER WITH ALOE VERA- ethyl alcohol liquid

My Medic Hand Sanitizer with Aloe Vera by

Drug Labeling and Warnings

My Medic Hand Sanitizer with Aloe Vera by is a Otc medication manufactured, distributed, or labeled by Sled Distribution, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol     72%

Purpose

Antiseptic

USE

• To decrease bacterica on the skin that could cause diease. 
• Signle use

Warning

• For external use only: hands
• Flammable: keep away from fire or flame.

When using this product

• Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
• Avoid contact with thoroughly with water.
• Avoid contact with broken skin.
• Do not inhale or ingest.

Stop use and ask a doctor,

• Irritaion and redness develop.
• Condition persists for more than 72 hours.

Other Information：

• Do not store above 110℉.
• May discolor some fabrics.
• Harmul to wood finishes and plastics.

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

Directions

• Wet hands thoroughly with product and allow to dry without wiping.
• For children under 6, use only under adult supervision.
• Not recommended for infants.

Inactive ingredients

Aloe Barbadensis Leaf Juice, Fragrance, Glycerin, Maltodextrin, Propylene Glycol, Triethanolamine Acrylates.C10-30 Alkyl Acrylate Cross Polymer, Water.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MY MEDIC HAND SANITIZER WITH ALOE VERA 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81417-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	72 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81417-002-01	2 g in 1 PACKAGE; Type 0: Not a Combination Product	04/27/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/27/2021

Labeler - Sled Distribution, LLC (079772888)

Establishment
Name	Address	ID/FEI	Business Operations
Sled Distribution, LLC		079772888	manufacture(81417-002)