AquaSource Hand Sanitizer

AquaSource Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

AQUASOURCE HAND SANITIZER- isopropyl alcohol 75% solution 
Blendpack, Inc.

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AquaSource Hand Sanitizer

Keep out of reach of children

Uses:

For hand sanitizing to decrease disease causing dermal bacteria. Recommended for repeated use. 

Active Ingredient: 

Isopropyl Alcohol 75%

Directions:

Place 1-2 pumps of product into palm. 

Rub hands together briskly until dry.

Children under 6 years of age should be supervised when using this product.

Warnings:

Flammable. Keep away from fire or flame

For external use only

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water

Stop use and ask doctor if irritation or redness develops, or if 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.

Inactive Ingredients:

Water, Glycerin, Hydrogen Peroxide

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AQUASOURCE HAND SANITIZER 
isopropyl alcohol 75% solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 86050-4750
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	750 g  in 1 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 86050-4750-1	3.79 L in 1 JUG; Type 0: Not a Combination Product	07/31/2024
2	NDC: 86050-4750-2	208.2 L in 1 DRUM; Type 0: Not a Combination Product	07/31/2024
3	NDC: 86050-4750-3	1041 L in 1 TANK; Type 0: Not a Combination Product	07/31/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/31/2024	11/05/2024

Labeler - Blendpack, Inc. (043362034)

Establishment
Name	Address	ID/FEI	Business Operations
Blendpack, Inc.		043362034	manufacture(86050-4750)

Revised: 11/2024

Document Id: 61ade288-4f3a-4a23-af72-f3a938d7300a

34390-5

Set id: ca235fda-2393-4f5f-b9a3-f1635a21a8c4

Version: 2

Effective Time: 20241105