Purge Hand Sanitizer

Manufacturer: OHAD PHARMACEUTICALS PRIVATE LIMITED
Effective date: 2020-09-17
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:30:10

Label at a glance#

ProductPurge Hand Sanitizer

Active ingredientALCOHOL

Label structure10 sections

Indications and uses

• hand sanitizer to decrease bacteria on the skin • recommended for repeated use • for use when soap and water are not available

Dosage and administration

• wet hands thoroughly with product and allow to dry without wiping • supervise children under 6 years of age when using this product to avoid swallowing • not recommended for infants

Storage and handling

• store between 15-30° C (59-86°F) • avoid freezing and excessive heat above 40° C (104° F) • may discolor some fabrics • harmful to wood finishes and plastics

Contacts and useful links#

PhoneLabel contact+1-770-840-0444

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• hand sanitizer to decrease bacteria on the skin

• recommended for repeated use

• for use when soap and water are not available

Warnings

WARNINGS SECTION

Flammable, keep away from fire/flame
For external use only

Do not use

• in children less than 2 months of age

• on open skin wounds

When using this product • do not get into eyes. In case of contact, rinse eyes thoroughly with water

• avoid contact with broken skin

• do not inhale or ingest

Stop use and ask a doctor if

• irritation and redness develop

• condition persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. 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

• supervise children under 6 years of age when using this product to avoid swallowing

• not recommended for infants

Other information

STORAGE AND HANDLING SECTION

• store between 15-30° C (59-86°F)

• avoid freezing and excessive heat above 40° C (104° F)

• may discolor some fabrics

• harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe vera, water, carbomer homopolymer, triethylamine, fragrance

Questions?

OTC - QUESTIONS SECTION

+1-770-840-0444

You may also report serious side effects to this phone number.

Mon-Fri 9:00 AM - 5:00 PM

SPL UNCLASSIFIED SECTION

Moisturizing with Aloe Vera

Distributed by:

HALPERN IMPORT COMPANY

Atlanta, GA 30360

Made in India

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79698-001-01	2022-01-28	C162847	48780-1	d6a99b39-9618-a426-e053-dadaa90af4c2	Purge™ ANTISEPTIC HAND SANITIZER
79698-001-02	2022-01-28	C162847	48780-1	d6a99b39-9618-a426-e053-dadaa90af4c2	Purge™ ANTISEPTIC HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79698-001-01	Purge Hand Sanitizer	59.2 mL in 1 BOTTLE	GEL	59.2		1
79698-001-02	Purge Hand Sanitizer	118.3 mL in 1 BOTTLE	GEL	118.3		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79698-001	PURGE HAND SANITIZER (ETHYL ALCOHOL) GEL [OHAD PHARMACEUTICALS PRIVATE LIMITED]	1	Legacy NDC, 2 package rows	20200925_896392bd-e853-44e2-9705-4a725704e0e0.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Purge Hand Sanitizer
Ethyl alcohol
ALCOHOL
ALOE VERA LEAF
WATER
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
TRIETHYLAMINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79698-001	79698-001-01, 79698-001-02

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
ALCOHOL	3K9958V90M	ACTIB
ALOE VERA LEAF	ZY81Z83H0X	IACT
WATER	059QF0KO0R	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
TRIETHYLAMINE	VOU728O6AY	IACT

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
2f5d1809-0b83-4bed-b4ae-0076516baf7c			896392bd-e853-44e2-9705-4a725704e0e0	2020-09-17	Warnings	Exact identifier spl id: 2f5d1809-0b83-4bed-b4ae-0076516baf7c spl set id: 896392bd-e853-44e2-9705-4a725704e0e0

Reported adverse events (FAERS/openFDA)#

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