Hand Sanitizer Pure Experience Liquid

Manufacturer: Absara Cosmetics S.A.P.I DE C.V.
Effective date: 2020-06-15
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:25:38

Label at a glance#

ProductHand Sanitizer Pure Experience Liquid

Active ingredientALCOHOL

Label structure7 sections

Dosage and administration

Apply the liquid 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

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.

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 liquid 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, *fragrance, dmdm hydantoin, aloe barbadensis extract.

*May contain this ingredient.

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product Label

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Hand Sanitizer Pure Experience Liquid
ALCOHOL
WATER
GLYCERIN
DMDM HYDANTOIN
ALOE VERA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70956-312	70956-312-01, 70956-312-04, 70956-312-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
DMDM HYDANTOIN	BYR0546TOW	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
3db39d6a-e4b0-4e4c-8b3f-aceb28346099			436ebef7-ac10-4a46-91e4-b4ffbe4f0272	2022-09-15	Warnings	Exact identifier spl set id: 436ebef7-ac10-4a46-91e4-b4ffbe4f0272

Reported adverse events (FAERS/openFDA)#

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