FDA.reportPublic FDA data

Project C.U.R.E Hand Sanitizer

Manufacturer
Abinter Labs LLC
Effective date
2021-08-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:38:19

Label at a glance#

ProductProject C.U.R.E Hand Sanitizer
Active ingredientAlcohol
Label structure9 sections

Dosage and administration

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

Storage and handling

Store below 106°F (41 °C). May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

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

Other information

STORAGE AND HANDLING SECTION

Store below 106°F (41 °C).

May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

PRINCIPAL DISPLAY PANEL - 250 ml Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

PRINCIPAL DISPLAY PANEL - 250 ml Bottle Label
PRINCIPAL DISPLAY PANEL - 250 ml Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81753-001-012024-01-19C16284748780-1e4f33bdf-b3bd-d8a0-e053-dadaa90a6e4eProject C.U.R.E Hand Sanitizer
81753-001-012022-07-29C16284748780-1e4f33bdf-b3bd-d8a0-e053-dadaa90a6e4eProject C.U.R.E Hand Sanitizer

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81753-00181753-001-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
Alcohol3K9958V90MACTIB
Propylene glycol6DC9Q167V3IACT
GlycerinPDC6A3C0OXIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
Water059QF0KO0RIACT
POLYETHYLENE GLYCOL 3005655G9Y8AQIACT
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%)2N8MDB79NAIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
669fcdff-a6c5-4368-a08b-a883102361199fd116f4-348f-4be5-928e-5454564530b12024-01-19WarningsExact identifier
spl set id: 9fd116f4-348f-4be5-928e-5454564530b1

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.