TALON ANTISEPTIC WIPES- alcohol, benzalkonium chloride cloth 
DOBOLV (QUANZHOU) PAPER CO., LTD

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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Talon® ANTISEPTIC WIPES

Drug Facts

Active ingredients

Alcohol 70% (V/V)

Benzalkonium Chloride 0.10% (W/V)

Purpose

Antiseptic

Uses

• for hand washing to decrease bacteria on the skin.

• Recommended for repeat use.

Warnings

For external use only. Flammable.

Keep away from heat or flame.

Do not use if you have been diagnosed by a physician as being allergic to any of the ingredients.

When using this product Keep out of eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if irritation or redness develops, and if condition persists for more than 71 hours.

Keep out of reach of children unless under adult supervision, If swallowed seek medical assistance.

Directions

• Wet hands thoroughly with product and allow to dry without rinse.

• Children under six years of age should be supervised when using this product.

Other information

• Store in a dry place away from fire.

• Manufacturing/Expiry Date: See package for details

Inactive ingredients

Aloe Vera Extract, Betaine, Citric acid, Dodecyl polyglucoside, Glycerol, Hexadecylpyridinium Chloride, Propanediol, Sodium citrate, Vitamin E, Water(Aqua).

P P E CARE KIT 

MADE BY Talon® INTERNATIONAL INC.

DISTRIBUTED BY:

Talon International, 21900 Burbank Blvd.,

Suite 101 Woodland Hills, CA 91367 USA

Made in China

Packaging

IMAGE

TALON ANTISEPTIC WIPES 
alcohol, benzalkonium chloride cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79891-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.10 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
BETAINE (UNII: 3SCV180C9W)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
GLYCERIN (UNII: PDC6A3C0OX)  
CETYLPYRIDINIUM CHLORIDE ANHYDROUS (UNII: 6BR7T22E2S)  
PROPANEDIOL (UNII: 5965N8W85T)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79891-003-1010 in 1 BAG10/30/2020
14.5 mL in 1 PACKAGE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A10/30/2020
Labeler - DOBOLV (QUANZHOU) PAPER CO., LTD (550022046)
Establishment
NameAddressID/FEIBusiness Operations
DOBOLV (QUANZHOU) PAPER CO., LTD550022046manufacture(79891-003)

Revised: 10/2020
Document Id: 1f3b792d-dd79-48e7-aacc-0de2d94b82d1
Set id: 4fb9edfb-dec9-40d1-9651-e2d0db09814a
Version: 1
Effective Time: 20201030
 
DOBOLV (QUANZHOU) PAPER CO., LTD