ALL DAY ULTRA HAND SANITIZER GEL- ethanol gel

All Day Ultra by

Drug Labeling and Warnings

All Day 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

purified water, isopropyl alcohol, glycerin, alpha-tocopherol acetate, aminomethylpropanol

QUESTIONS

Questions?Call 1-844-929-9199

SPL UNCLASSIFIED SECTION

Distributed by: General Resources, LLC

1430 Haines Avenue, Ste. 105-186

Rapid City, South Dakota 57701

www.alldayprotect.com

* 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.

PRINCIPAL DISPLAY PANEL

24 HR

ALL DAY ULTRA

HAND SANITIZER GEL

ALCOHOL-BASED

INSTANTLY KILLS 99.99% OF TESTED GERMS*

FRAGRANCE-FREE

2 fl oz (60 mL)

Proudly made in the USA

INGREDIENTS AND APPEARANCE

ALL DAY ULTRA  HAND SANITIZER GEL
ethanol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70481-112
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	72 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70481-112-06	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/11/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	02/11/2020

Labeler - General Resources LLC (080140979)