HAND SANITIZER GEL- hand sanitizer gel gel 
LS Promotions Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Hand Sanitizer Gel - Single Use Packet

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

ABL1430 Hand Sanitizer Gel 101.jpg

HAND SANITIZER GEL 
hand sanitizer gel gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72449-101
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72449-101-012.9 mL in 1 PACKET; Type 0: Not a Combination Product03/16/2020
2NDC:72449-101-025.9 mL in 1 PACKET; Type 0: Not a Combination Product03/16/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/16/2020
Labeler - LS Promotions Inc. (024818391)
Registrant - LS Promotions Inc. (024818391)
Establishment
NameAddressID/FEIBusiness Operations
LS Promotions Inc.024818391manufacture(72449-101)

Revised: 3/2020
Document Id: a0fc7c8c-133f-275d-e053-2995a90a6af6
Set id: a0fc7c8c-133e-275d-e053-2995a90a6af6
Version: 1
Effective Time: 20200316
 
LS Promotions Inc.