Porago Hand Sanitizer

Manufacturer: Puraall LLC | GUANGZHOU ORCHARD AROMATHERAPY & SKIN CARE CO.,LTD
Effective date: 2020-05-11
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:21:01

Label at a glance#

ProductPurago Hand Sanitizer

Active ingredientALCOHOL

Label structure7 sections

Indications and uses

to decrease bacteria on the skin that could cause disease recommended for repeated use

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping for children under 6, use only under adult supervision not recommended for infants

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin that could cause disease
recommended for repeated use

Warnings

WARNINGS SECTION

For external use only: hands

Flammable, keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
avoid contact with broken skin
do not inhale or ingest

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop
condition persist for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product and allow to dry without wiping
for children under 6, use only under adult supervision
not recommended for infants

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Aloe Barbadensis Leaf Extract, Acrylate/C10-30 alkyl Acrylate Crosspolymer, Tetrahydroxypropyl Ethylenediamine

Other Information

SPL UNCLASSIFIED SECTION

do not store above 105°F
may discolor some fabrics
harmful to wood finishes and plastics

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label5

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1305100	ethanol 75 % Topical Gel	PSN	3
1305100	ethanol 0.75 ML/ML Topical Gel	SCD	3
1305100	ethanol 75 % Topical Gel	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76812-004-00	2023-01-30	C162847	48780-1	f386c64a-43f4-0266-e053-dadaa90a7c1a	Purago Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76812-004-00	Purago Hand Sanitizer	250 mL in 1 BOTTLE	GEL	250		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76812-004	PURAGO HAND SANITIZER (ALCOHOL) GEL [PURAALL LLC]	3	Legacy NDC, 1 package rows	20200711_f6178324-30fc-4e3c-9606-90fb0ce45ddc.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Purago Hand Sanitizer
ALCOHOL
WATER
ALOE VERA LEAF
EDETOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76812-004	76812-004-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
EDETOL	Q4R969U9FR	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
a55edebe-7ec1-5286-e053-2995a90a6c88			f6178324-30fc-4e3c-9606-90fb0ce45ddc	2020-05-11	Warnings	Exact identifier spl id: a55edebe-7ec1-5286-e053-2995a90a6c88 spl set id: f6178324-30fc-4e3c-9606-90fb0ce45ddc

Reported adverse events (FAERS/openFDA)#

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