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All Day Hand Sanitizer Ultra

Medically reviewed on August 25, 2016

Dosage form: liquid
Ingredients: ALCOHOL 720g in 1L
Labeler: General Resources LLC
NDC Code: 70481-111

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.

All Day Hand Sanitizer Ultra

Drug Facts

Active ingredient

Ethyl Alcohol 72%

Purpose

Antiseptic

Uses

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

Warnings

For external use only

Flammable. Keep away from fire or flame.

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

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 ULTRA 
ethanol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70481-111
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL720 g  in 1 L
Inactive Ingredients
Ingredient NameStrength
WATER 
Packaging
#Item CodePackage Description
1NDC:70481-111-010.01 L in 1 BOTTLE, SPRAY
2NDC:70481-111-251 L in 1 BAG
3NDC:70481-111-060.06 L in 1 BOTTLE, SPRAY
4NDC:70481-111-240.237 L in 1 BOTTLE, SPRAY
5NDC:70481-111-050.05 L in 1 BOTTLE, SPRAY
6NDC:70481-111-321 L in 1 BOTTLE, SPRAY
7NDC:70481-111-401 L in 1 BOTTLE
8NDC:70481-111-263.8 L in 1 JUG
9NDC:70481-111-5018.9 L in 1 PAIL
10NDC:70481-111-55208 L in 1 CONTAINER
11NDC:70481-111-991041 L in 1 CONTAINER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/25/2016
Labeler - General Resources LLC (080140979)

 
General Resources LLC

Further information

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

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