FDA.reportPublic FDA data

Hand Sanitizer Rinse Free

Manufacturer
Absara Cosmetics S.A.P.I DE C.V.
Effective date
2020-05-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:30:51

Label at a glance#

ProductHand Sanitizer Rinse Free
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin.

Dosage and administration

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

Storage and handling

Store below 106ºF (41 ºC). May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

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.

OTC - WHEN USING SECTION

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.

OTC - STOP USE SECTION

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 106ºF (41 ºC). May discolor certain fabrics or surfaces.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

demineralized water, glycerin, carbomer, triethanolamine, dmdm hydantoin, aloe barbadensis extract, iodopropynyl butylcarbamate, butylene glycol.

Package Labeling: 70956-420-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70956-420-0170956-420-01

Package Labeling: 70956-420-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70956-420-0270956-420-02

Package Labeling: 70956-420-03

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70956-420-0370956-420-03

Package Labeling: 70956-420-04

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70956-420-0470956-420-04

Package Labeling: 70956-420-05

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70956-420-0570956-420-05

Package Labeling: 70956-420-06

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70956-420-0670956-420-06

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70956-42070956-420-01, 70956-420-02, 70956-420-03, 70956-420-04, 70956-420-05, 70956-420-06, 70956-420-07, 70956-420-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
DMDM HYDANTOINBYR0546TOWIACT
ALOE VERA LEAFZY81Z83H0XIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML · Source PDF

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
e45d25a9-afc9-b7af-e053-2a95a90a3b384e0dfb0e-36fd-471b-beff-c60583b2b4222022-07-21WarningsExact identifier
spl set id: 4e0dfb0e-36fd-471b-beff-c60583b2b422

Reported adverse events (FAERS/openFDA)#

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