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All Day Hand Sanitizer

Medically reviewed by Drugs.com. Last updated on Oct 27, 2019.

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 0.13g in 1mL
Labeler: General Resources LLC
NDC Code: 70481-001

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

All Day Hand Sanitizer

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Uses

  • Hand sanitizing to help reduce bacteria on the skin
  • Recommended for repeated use

Warnings

For external use only

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

​Stop use and ask a doctor if irritation or redness appears and lasts

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Apply liberally to hands and gently rub until dry.

Other information

Store above 0°C (32°F)

Inactive ingredients

water, fragrances, ethyl alcohol

Questions? Call 1-605-646-4060

* Patented formula effectively eliminates 99.99% of harmful germs, bacteria and viruses in as little as 15 seconds; antimicrobial protection for up to 24 hours.

Distributed by: General Resources, LLC

1430 Haines Avenue, Ste. 105-186

Rapid City, South Dakota 57701

www.gen-resources.com

TRICLOSAN, SULFATE AND PARABEN-FREE

CLEANS

PROTECTS

MOISTURIZERS

All Day

ANTIBACTERIAL HAND SANITIZER

WATER-BASED

Antimicrobial protection against 99.99% of all germs, bacteria and viruses*

2 fl oz (60 mL)

Proudly made in the USA

ALL DAY HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70481-001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE0.13 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
ALCOHOL 
Packaging
#Item CodePackage Description
1NDC:70481-001-0110 mL in 1 BOTTLE, SPRAY
2NDC:70481-001-0550 mL in 1 BOTTLE, SPRAY
3NDC:70481-001-0660 mL in 1 BOTTLE, SPRAY
4NDC:70481-001-24240 mL in 1 BOTTLE, SPRAY
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/01/2016
Labeler - General Resources LLC (080140979)

 
General Resources LLC

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