PURGE HAND SANITIZER- ethyl alcohol gel

Purge Hand Sanitizer by

Drug Labeling and Warnings

Purge Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by OHAD PHARMACEUTICALS PRIVATE LIMITED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl alcohol 70% v/v

Purpose

Antiseptic

Uses

hand sanitizer to decrease bacteria on the skin

 recommended for repeated use

 for use when soap and water are not available

Warnings

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center
right away.

Directions

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

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

aloe vera, water, carbomer homopolymer, triethylamine, fragrance

Questions?

+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

INGREDIENTS AND APPEARANCE

PURGE HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79698-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TRIETHYLAMINE (UNII: VOU728O6AY)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79698-001-01	59.2 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/17/2020
2	NDC: 79698-001-02	118.3 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/17/2020

Labeler - OHAD PHARMACEUTICALS PRIVATE LIMITED (877233487)

Establishment
Name	Address	ID/FEI	Business Operations
OHAD PHARMACEUTICALS PRIVATE LIMITED		877233487	manufacture(79698-001)