BIG WIPES MULTI-PURPOSE- benzalkonium chloride cloth 
Sycamore USA 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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BIG WIPES

MULTI-PURPOSE

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

Ceans hands and reduces bacteria on the skin

Warnings

For external use only

When using this product do not use in or around eyes. May irritate eyes.

If IN EYES rinse well for 15 minutes

KEEP OUT OF REACH OF CHILDREN

Directions

Open foil seal and pull the center wipe through the lid

Inactive ingredients

WATER (AQUA), DIMETHYL SUCCINATE, DIMETHYL GUTARATE, DIMETHYL ADIPATE, DIMETHYL METHYLGLUTARATE. POLYSORBATE-80, POLYSORBATE-20, DIDECYLDIMONIUM CHLORIDE, GLYCERIN, METHYL SOYATE, PEG-75 LANOLIN, ALCOHOL, CITRIC ACID, SODIUM CITRATE, ALOE BARBADENSIS LEAF JUICE, TOCOPHERYL ACETATE (VITAMIN E), PROPANEDIOL, PARFUM.

Questions?

Call (770) 628-0286 or visit www.bigwipesusa.com

BIG WIPES

MULTI-PURPOSE

ANTIBACTERIAL HAND WIPES

PRO+

CLEANS

PAINT

ADHESIVE

SILICONE

POLY FOAM

GAP FILL

OIL

GRIME

and MORE FROM

YOUR HANDS

4x4 FORMULA

TOUGH ON

GRIME

KIND TO YOUR HANDS

NDC # 79705-002-04

ANTIBACTERIAL

check mark

Hand Wipes

NSF

Nonfood Compound

E4

DERMATOLOGICALLY TESTED

80

WIPES (8" x 12")

HAND SANITIZER WIPES

container label

BIG WIPES MULTI-PURPOSE 
benzalkonium chloride cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79705-002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
METHYL SOYATE (UNII: 808DL597QP)  
DIMETHYL GLUTARATE (UNII: 1I9VFA346P)  
DIMETHYL METHYLGLUTARATE (UNII: 728OFW5M9G)  
WATER (UNII: 059QF0KO0R)  
DIMETHYL SUCCINATE (UNII: 914I2127JR)  
DIMETHYL ADIPATE (UNII: BY71RX0R62)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
PROPANEDIOL (UNII: 5965N8W85T)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)  
PEG-75 LANOLIN (UNII: 09179OX7TB)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79705-002-014 mL in 1 POUCH; Type 0: Not a Combination Product08/31/2020
2NDC:79705-002-03110 mL in 1 CANISTER; Type 0: Not a Combination Product08/31/2020
3NDC:79705-002-04310 mL in 1 CANISTER; Type 0: Not a Combination Product08/31/2020
4NDC:79705-002-061161 mL in 1 CANISTER; Type 0: Not a Combination Product08/31/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/31/202010/31/2025
Labeler - Sycamore USA Inc. (078589316)
Establishment
NameAddressID/FEIBusiness Operations
WET NAPS LTD.514650902manufacture(79705-002)

Revised: 11/2022
Document Id: ee26f5f8-cd7f-60fb-e053-2a95a90a877a
Set id: ae326410-17f1-2e72-e053-2a95a90a15a2
Version: 3
Effective Time: 20221123
 
Sycamore USA Inc.