GERMEND- ethyl alcohol gel

GermEnd by

Drug Labeling and Warnings

GermEnd by is a Otc medication manufactured, distributed, or labeled by Lee's Collection Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 75% in 60ml

Purpose

Antiseptic

INDICATIONS & USAGE

Use  Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warning

For external use only: Hands

Flammable: keep away from fire and flame.

Use with caution for people with alcohol allergies.

When using this product  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 irritation and redness develop and condition persists for more than 72 hours.

Do not use  with children less than 2 months of age

                   on open skin wounds

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

DOSAGE & ADMINISTRATION

Directions Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervise. Not recommended for infants.

STORAGE AND HANDLING

Other information  Store between 15-30C (59-86F)  Avoid freezing and excessive heat above 40C (104F)

INACTIVE INGREDIENT

Inactive ingredients : aqua,carbomer,aminomethyl propanol,vitamin E.

SPL UNCLASSIFIED SECTION

Kills 99.99% of germs

Effective at eliminating over 99.99% of common harmful germs and bacteria.

Distributed by   Lee's Collection Inc.

                          S. El Monte , CA 91733 USA

Made in China

Packaging

INGREDIENTS AND APPEARANCE

GERMEND 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74027-300
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74027-300-06	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/08/2020
2	NDC: 74027-300-13	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/08/2020
3	NDC: 74027-300-10	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/08/2020
4	NDC: 74027-300-12	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/08/2020

Labeler - Lee's Collection Inc. (022215540)