ALL DAY HAND SANITIZER ULTRA- ethanol liquid

All Day Hand Sanitizer Ultra by

Drug Labeling and Warnings

All Day Hand Sanitizer Ultra by is a Otc medication manufactured, distributed, or labeled by General Resources LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredient

Ethyl Alcohol 72%

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Uses

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

WARNINGS

Warnings

For external use only

Flammable. Keep away from fire or flame.

WHEN USING

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

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Directions

Apply liberally to hands and gently rub until dry.

STORAGE AND HANDLING

Other information

Store above 0°C (32°F)

INACTIVE INGREDIENT

Inactive ingredients

water, fragrances

QUESTIONS

Questions?Call 1-605-646-4060

SPL UNCLASSIFIED SECTION

* 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

PRINCIPAL DISPLAY PANEL

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

INGREDIENTS AND APPEARANCE

ALL DAY HAND SANITIZER ULTRA 
ethanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70481-111
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	720 g  in 1 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70481-111-01	0.01 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/25/2016
2	NDC: 70481-111-25	1 L in 1 BAG; Type 0: Not a Combination Product	08/25/2016
3	NDC: 70481-111-06	0.06 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/25/2016
4	NDC: 70481-111-24	0.237 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/25/2016
5	NDC: 70481-111-05	0.05 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/25/2016
6	NDC: 70481-111-32	1 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/25/2016
7	NDC: 70481-111-40	1 L in 1 BOTTLE; Type 0: Not a Combination Product	08/25/2016
8	NDC: 70481-111-26	3.8 L in 1 JUG; Type 0: Not a Combination Product	08/25/2016
9	NDC: 70481-111-50	18.9 L in 1 PAIL; Type 0: Not a Combination Product	08/25/2016
10	NDC: 70481-111-55	208 L in 1 CONTAINER; Type 0: Not a Combination Product	08/25/2016
11	NDC: 70481-111-99	1041 L in 1 CONTAINER; Type 0: Not a Combination Product	08/25/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/25/2016

Labeler - General Resources LLC (080140979)