Project C.U.R.E Hand Sanitizer

Project C.U.R.E Hand Sanitizer by

Drug Labeling and Warnings

Project C.U.R.E Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Abinter Labs LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PROJECT C.U.R.E HAND SANITIZER- alcohol gel 
Abinter Labs LLC

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Project C.U.R.E Hand Sanitizer

DRUG FACTS

Active ingredient

Ethyl alcohol 70% v/v

Purpose

Antimicrobial

Use

Hand sanitizer to help reduce bacteria on the skin.

Warnings

Flammable. Keep away from fire or flame. For external use only. Do not ingest, if swallowed seek medical help. Avoid contact with eyes.

Keep out of reach of children. Children under 6yrs old to use under adult supervision. In case of irritation, discontinue use and consult your doctor.

Directions

Apply the gel on the hands and rub gently for 20 seconds until the product evaporates.

Other information

Store below 106°F (41 °C).

May discolor certain fabrics or surfaces.

Inactive ingredients

Water, propylene glycol, glycerin, aloe barbadensis extract, tocopheryl acetate, fragrance, PEG-6, Acrylates/Vinyl Isodecanoate Crosspolymer.

PRINCIPAL DISPLAY PANEL - 250 ml Bottle Label

projectc.u.r.e.

www.projectcure.org

HAND SANITIZER
70% ALCOHOL
NDC: 81753-001-01

Donated by: Benevolent Healthcare Foundation (dba Project C.U.R.E.)
Manufactured in: Abinter Labs LLC Magnolia, TX 77354

MADE IN
USA

8.45 FL OZ
250 ml

PROJECT C.U.R.E HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81753-001
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
Propylene glycol (UNII: 6DC9Q167V3)
Glycerin (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
Water (UNII: 059QF0KO0R)
POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81753-001-01	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/16/2021	01/17/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph drug	M003	08/16/2021	01/17/2024

Labeler - Abinter Labs LLC (117981053)

Establishment
Name	Address	ID/FEI	Business Operations
Abinter Labs LLC		117981053	PACK(81753-001)

Revised: 1/2024

Document Id: 669fcdff-a6c5-4368-a08b-a88310236119

34390-5

Set id: 9fd116f4-348f-4be5-928e-5454564530b1

Version: 2

Effective Time: 20240119