TOUCHPOINT WIPES FRAGRANCE FREE SANITIZING WIPES- benzalkonium chloride cloth 
Innocore Sales & Marketing Inc

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Touchpoint Wipes Fragrance Free

Sanitizing Wipes

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13 %

Purpose

Antimicrobal

Use

Hand sanitizer to help reduce bacteria on the skin.

Recommended for repeated use.

Warnings

For external use only.

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly in water.

Discontinue use if irritation and redness develop. If conditions persist for more than 72 hours, consult a physician.

If swallowed get medical help or contact a poison control center immediately.

Keep out of reach of children.

Directions

Inactive ingredients

Benzoic Acid, Caprylyl/Capryl Oligoglucoside, Dehydroacetic Acid, Phenoxyethanol, Poly(Laurylglucoside)-7, Propylene Glycol, Water

1500 Wipe Pouch Label

Touch

Point™

Sanitizing Wipes

1500 Wipes • 8"x 6"

Fragrance Free

Kills 99.99%

of most common germs that may cause illness

PRINCIPAL DISPLAY PANEL - 1500 Wipe Pouch Label

TOUCHPOINT WIPES FRAGRANCE FREE  SANITIZING WIPES
benzalkonium chloride cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70924-002
Route of AdministrationCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)  
POLY(LAURYLGLUCOSIDE)-7 (UNII: VB00RDE21R)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70924-002-022 in 1 BOX09/09/2016
1NDC:70924-002-011500 in 1 POUCH; Type 0: Not a Combination Product
2NDC:70924-002-042 in 1 BOX12/11/2018
2NDC:70924-002-031800 in 1 POUCH; Type 0: Not a Combination Product
3NDC:70924-002-062 in 1 BOX12/11/2018
3NDC:70924-002-052400 in 1 POUCH; Type 0: Not a Combination Product
4NDC:70924-002-092 in 1 BOX12/11/2018
4NDC:70924-002-07400 in 1 POUCH; Type 0: Not a Combination Product
5NDC:70924-002-116 in 1 BOX12/11/2018
5NDC:70924-002-10320 in 1 CANISTER; Type 0: Not a Combination Product
6NDC:70924-002-136 in 1 BOX10/16/2019
6NDC:70924-002-12150 in 1 CANISTER; Type 0: Not a Combination Product
7NDC:70924-002-152 in 1 BOX11/11/2019
7NDC:70924-002-142200 in 1 POUCH; Type 0: Not a Combination Product
8NDC:70924-002-172 in 1 BOX09/21/2022
8NDC:70924-002-16650 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)09/09/2016
Labeler - Innocore Sales & Marketing Inc (201152597)

Revised: 12/2023
Document Id: 0c454b7b-57e1-327e-e063-6394a90a7143
Set id: e805a12d-2bd8-4331-bd81-02c99d057acf
Version: 8
Effective Time: 20231211
 
Innocore Sales & Marketing Inc