Advanced Hand Sanitizer by Logomark Inc Advanced Hand Sanitizer

Advanced Hand Sanitizer by

Drug Labeling and Warnings

Advanced Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Logomark Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ADVANCED HAND SANITIZER- alcohol gel 
Logomark Inc

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Advanced Hand Sanitizer

Drug Facts

Active ingredient

Ethyl Alcohol 75%(V/V)

Purpose

Antiseptic

Use

For handwashing to decrease bacteria on the skin.

Warnings

For external use only

Flammable. Keep away from fire or flame.

When using this product

avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

irritation or rash develops and continues 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

• Tear open packet and take a palmful of product in one hand.
• Spread on both hands and rub into skin until dry (approximately 1 to 2 minutes)
  

Other information

• Do not store above 86°F (30°C)
• May discolor some fabrics
• Harmful to wood finishes and plastics

Inactive ingredients

Acrylates/C10-30 Akyl Acrylate Crosspolymer, Aminomethyl Propanol, Aqua (Water), Fructose, Glycerin, Inulin, Panthenol, Sodium Hyaluronate,
Squalane, Tocopheryl Acetate

Package Labeling

ADVANCED HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76806-018
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
WATER (UNII: 059QF0KO0R)
FRUCTOSE (UNII: 6YSS42VSEV)
GLYCERIN (UNII: PDC6A3C0OX)
INULIN (UNII: JOS53KRJ01)
PANTHENOL (UNII: WV9CM0O67Z)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
SQUALANE (UNII: GW89575KF9)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76806-018-01	2 mL in 1 BAG; Type 0: Not a Combination Product	06/20/2020	01/31/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/20/2020	01/31/2026

Labeler - Logomark Inc (829978766)

Revised: 1/2024

Document Id: 0fb4d2e9-7a53-0a6f-e063-6394a90aa75d

34390-5

Set id: de816283-b4a6-4325-a717-b673f59b74c9

Version: 2

Effective Time: 20240124

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