ANTIBACTERIAL WIPES- benzalkonium chloride swab 
ERC Acquisition, 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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Drug Facts

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antimicrobial

Uses

Warnings

For external use only

Do not use if

you are allergic to any of this product

When using this product

avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor

If irritation or redness develops, or if condition persists for more than 72 hours.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Adults and Children 2 years and over: apply to hands and face. Allow to dry without wiping.

Children under 2 years: ask a doctor before use

To dispense: pull tab and remove large cover. Insert triangular threading loop through slits in cover. Do not push finger through the opening. Thread first sheet in center or roll through loop. Replace cover. Pull loop back through opening. Pull each sheet up and slightly to the side. Dispose of wipe in trash. Do not flush.

Other information

Store below 95 o​F (35 oC). keep closed tightly. May discolor certain fabric or surfaces

Inactive ingredients

Water, SD Alcohol 40, Phenoxyethanol, Decyl Glucoside, Potassium Sorbate, Sodium Benzoate, Disodium EDTA,  Citric Acid, Aloe Barbadensis  (Aloe)  Leaf Extract, Fragrance.

Principal Display Panel

NDC 71293-020-01

2000 count

ERC

ERC WIPING PRODUCTS

KILLS 99.9% OF GERMS

ANTIBACTERIAL WIPES

Cleans, Disinfects and Deodorizes

2000 Wipes per roll

ercwipe.com 800-225-9473

Label

ANTIBACTERIAL WIPES 
benzalkonium chloride swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71293-020
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71293-020-012000 in 1 BAG03/16/2017
11 g in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/16/2017
Labeler - ERC Acquisition, Inc (019312339)
Registrant - ERC Acquisition, Inc (019312339)
Establishment
NameAddressID/FEIBusiness Operations
Precare Corp.117111327manufacture(71293-020)

Revised: 11/2022
Document Id: eea10c57-a528-9152-e053-2a95a90a0107
Set id: dc6c39af-447c-481a-98b5-33b8f09b83bc
Version: 4
Effective Time: 20221129
 
ERC Acquisition, Inc