EAGLE PROMOTIONS- hand sanitizer 128oz gel

Eagle Promotions by

Drug Labeling and Warnings

Eagle Promotions by is a Otc medication manufactured, distributed, or labeled by Nutrix International, LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT[S]

Alcohol 70% v/v

PURPOSE

Antiseptic

USE[S]

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

WARNINGS

For external use only. Flammable. Keep away from heat or flame.

DO NOT USE

• On children less than 2 months of age. On open skin wounds.

WHEN USING

Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

If irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help, or contact a Poison Control Center right away.

DIRECTIONS

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age. When using this product avoid swallowing.

OTHER INFORMATION

• Store between 15-30°C (59-86°F) Avoid freezing and excessive heat above 40°C (104°F)

INACTIVE INGREDIENTS

Water (Aqua), Propylene Glycol, Glycerin, Methyl Hydroxypropyl Cellulose, Melaleuca Alternifolia (Tea Tree) Leaf Oil.

DISPLAY PANEL

Label

INGREDIENTS AND APPEARANCE

EAGLE PROMOTIONS 
hand sanitizer 128oz gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73333-128
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 g  in 3974 g

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	0.01 g  in 3974 g
WATER (UNII: 059QF0KO0R)	0.273 g  in 3974 g
HYPROMELLOSES (UNII: 3NXW29V3WO)	0.007 g  in 3974 g
TEA TREE OIL (UNII: VIF565UC2G)	0.002 g  in 3974 g
GLYCERIN (UNII: PDC6A3C0OX)	0.008 g  in 3974 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73333-128-01	3974 g in 1 BOTTLE; Type 0: Not a Combination Product	07/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/08/2020

Labeler - Nutrix International, LLC. (117341868)

Establishment
Name	Address	ID/FEI	Business Operations
Nutrix International, LLC.		117341868	manufacture(73333-128) , pack(73333-128) , label(73333-128)