TRIPLE SHIELD Alcohol-Free  HAND SANITIZER GEL

TRIPLE SHIELD HAND SANITIZER by

Drug Labeling and Warnings

TRIPLE SHIELD HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Enviro Specialty Chemicals Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

TRIPLE SHIELD HAND SANITIZER- benzalkonium chloride gel 
Enviro Specialty Chemicals 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.

----------

TRIPLE SHIELD Alcohol-Free HAND SANITIZER GEL

Drug Facts

Active Ingredient: Benzalkonium Chloride 0.13%

Purpose: Antiseptic/Hand & Skin Sanitizer

Uses: Hand Sanitizer to help decrease bacteria on the skin -

Recommended for repeated use.

Warnings:

Do not freeze. For external use only.

Do not use in ears, eyes or mouth.

 When using this product, avoid contact with the eyes. In case of contact, flush eyes with water.

Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

Children should be supervised when using this product.

Directions: Apply liberally to the palms of the hands. Rub into skin until dry. Recommended for repeat use

Inactive Ingredients:

Aloe Barbadensis leaf extract, Aqua, Citric Acid, Caprylyl Glucoside, Hydroxyethyl Cellulose, Polyhexanide, Phenoxyethanol, Triethoxysilylpropyl

Steardimonium Chloride.

OTHER INFORMATION:

Store in a cool dry place below 104˚F (40˚C)

Questions? +1(888) 397-8731

FAST ACTING

15 SECOND FORMULA

WITH SOOTHING ALOE VERA

Long-lasting, alcohol-free protection from germs for your hands

KILLS 99.99% OF GERMS

Formulated and enhanced with

Zetrisil

FORMULATED IN THE USA | MADE IN CHINA

DISTRIBUTED BY TRIPLEROOT®

10004 WURZBACH RD.#104

SAN ANTONIO, TX 78230

www.tripleshieldusa.com

sales@tripleroot.com

Packaging

IMAGE

IMAGE

IMAGE

TRIPLE SHIELD HAND SANITIZER 
benzalkonium chloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 71884-033
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)  
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
POLIHEXANIDE (UNII: 322U039GMF)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE (UNII: XGN40YQC7B)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 71884-033-08244 mL in 1 BOTTLE; Type 0: Not a Combination Product08/26/202012/09/2021
2NDC: 71884-033-123780 mL in 1 BOTTLE; Type 0: Not a Combination Product08/26/202012/09/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/26/202012/09/2021
Labeler - Enviro Specialty Chemicals Inc (202621850)

Revised: 12/2021
Document Id: daa4f026-0ab5-4ad1-9a7e-4c917fb132b3
Set id: 90570df9-876a-498b-82f2-e86db9328cd5
Version: 2
Effective Time: 20211209