Hand Sanitizer Gel by LS Promotions Inc. HAND SANITIZER GEL gel

Hand Sanitizer Gel by

Drug Labeling and Warnings

Hand Sanitizer Gel by is a Otc medication manufactured, distributed, or labeled by LS Promotions Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Drug Facts

Active Ingredient

Ethanol 62%

PURPOSE

ANTISEPTIC

USES

TO HELP DECREASE BACTERIA ON HANDS

WARNINGS

FOR EXTERNAL USE ONLY. FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME

WHEN USING THIS PRODUCT

KEEP OUT OF EYES. IN CASE OF CONTACT WITH EYES, FLUSH THOROUGHLY WITH WATER AND THEN SEEK MEDICAL ADVICE.

STOP USE AND ASK A DOCTOR

IF IRRITATION OR REDNESS DEVELOPS

KEEP OUT OF REACH OF CHILDREN

IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

DIRECTIONS

PLACE ENOUGH PRODUCT IN YOUR PALM TO THOROUGHLY COVER HAND. RUB HANDS TOGETHER BRISKLY UNTIL DRY. FOR CHILDREN UNDER 6 YEARS OLD, USE ADULT SUPERVISION.

OTHER INFORMATION

DO NOT STORE ABOVE 100° F.

INACTIVE INGREDIENTS

Inactive Ingredients: water, glycerin, propylene glycol, isopropyl myristate, tocopheryl acetate, carbomer, triethanolamine, fragrance

QUESTIONS OR COMMENTS?

CALL WEEKDAYS FROM 9AM TO 5PM EST AT 631-231-2300
WWW.LANCOPROMO.COM

PDP_ Packet

INGREDIENTS AND APPEARANCE

HAND SANITIZER GEL 
hand sanitizer gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72449-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER 1342 (UNII: 809Y72KV36)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72449-101-01	2.9 mL in 1 PACKET; Type 0: Not a Combination Product	03/16/2020
2	NDC: 72449-101-02	5.9 mL in 1 PACKET; Type 0: Not a Combination Product	03/16/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/16/2020

Labeler - LS Promotions Inc. (024818391)

Registrant - LS Promotions Inc. (024818391)

Establishment
Name	Address	ID/FEI	Business Operations
LS Promotions Inc.		024818391	manufacture(72449-101)