LTD GLOBAL TRADING 70% ALCOHOL HAND SANITIZER- alcohol gel 
LTD ENTERPRISES DISTRIBUTION, 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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LTD Global Trading 70% Alcohol Gel Hand Sanitizer

LTD Global Trading 70% Alcohol Gel Hand Sanitizer

Drug Facts

Active Ingredient(s)

Alcohol 70% v/v.

Purpose

Antiseptic

Use

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

Warnings

Flammable. Keep away from source of heat, fire or flame.

For external use only.

Not for Consumption. Keep the product away from sunight.

When using this product

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if irritation or redness develops and lasts as these may be signs of a serious condition.

Keep out of reach of children

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

Directions

Storage

Inactive ingredients

Purified water, carbomer, glycerine, triethanolamine

Package Label - Principal Display Panel

NDC: 78072-400-

Made in Mexico

Label

Label

Label

LabelLabel

LTD GLOBAL TRADING 70% ALCOHOL HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78072-400
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
GLYCERIN (UNII: PDC6A3C0OX)  
TROLAMINE (UNII: 9O3K93S3TK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:78072-400-103790 mL in 1 JUG; Type 0: Not a Combination Product06/18/2020
2NDC:78072-400-11118 mL in 1 BOTTLE; Type 0: Not a Combination Product06/18/2020
3NDC:78072-400-23237 mL in 1 BOTTLE; Type 0: Not a Combination Product06/18/2020
4NDC:78072-400-47473 mL in 1 BOTTLE; Type 0: Not a Combination Product06/18/2020
5NDC:78072-400-94946 mL in 1 BOTTLE; Type 0: Not a Combination Product06/18/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/18/2020
Labeler - LTD ENTERPRISES DISTRIBUTION, INC. (092505379)
Registrant - LTD ENTERPRISES DISTRIBUTION, INC. (092505379)

Revised: 7/2020
Document Id: aa807d41-cf32-e1d6-e053-2a95a90a9912
Set id: a862e415-8362-90b7-e053-2a95a90a8f1c
Version: 4
Effective Time: 20200715
 
LTD ENTERPRISES DISTRIBUTION, INC.