Hand Sanitizer Rinse Free

Manufacturer
Absara Cosmetics S.A.P.I DE C.V.
Effective date
2022-02-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:08:31

Label at a glance#

ProductHand Sanitizer Rinse Free
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

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

Label contents#

Full prescribing information#

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 

OTC - DO NOT USE SECTION

ingest, if swallowed seek medical help. Avoid contact with eyes.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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:

SPL UNCLASSIFIED SECTION

Store below 106°F (41°C).

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.

OTC - QUESTIONS SECTION

For questions or comments call tel 832-559-3959

Package Labeling: 70956-001-20

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:70956-001-19

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling:70956-001-10

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70956-00170956-001-20, 70956-001-19, 70956-001-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

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
e45cc29d-8644-5da4-e053-2a95a90ad9a0a37d46c5-8116-5bd6-e053-2a95a90a861a2022-07-21WarningsExact identifier
spl set id: a37d46c5-8116-5bd6-e053-2a95a90a861a

Reported adverse events (FAERS/openFDA)#

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