PL-0591- flexi hand sanitizer gel

PL-0591 by

Drug Labeling and Warnings

PL-0591 by is a Otc medication manufactured, distributed, or labeled by Broder Bros Co.,, Prime Resources Corp, Yuyao Jessie Commodity Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol (62%)

Purpose

Antiseptic

Use

for hand-washing to decrease bacteria on skin

Warnings

For external use only.

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Warnings

Flammable. Keep away from heat and flame.

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Warnings

Do not use in the eyes. In case of contact, rinse eyes throughly with water.

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Warnings

Stop use & ask a doctor if irritation and redness develops and persists for more than 72 hours.

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Warnings

Keep out of reach of children if swallowed, get medical help or contact a Poinson Control Center right away.

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Directions

• Wet hands throughly with product, briskly rub together until dry.
• Always supervise children in use of this product.

Other Information

• Store at 68º to 77°F (20° to 25°C)
• May discolor certain fabrics

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Inactive ingredients

Aloe Barbadensis oil, Fragrance, Propylene glycol, Tocopherol, Water(Aqua)

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Questions?

1-800-873-7746 M-F 8am-5pm EST

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OTHER SAFETY INFORMATION

Lot no:

Use by:

Made in China

Distributed by: Prime Resource Corp Bridgeport, CT 06610

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Hand Sanitizer

Hand Sanitizer

Net wt. 1 FL OZ (29.5mL)

Hand Sanitizer

Hand Santizer

2 FL OZ (59 mL)

INGREDIENTS AND APPEARANCE

PL-0591 
flexi hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71513-059
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 62 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TOCOPHEROL (UNII: R0ZB2556P8)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71513-059-01	30 mL in 1 POUCH; Type 0: Not a Combination Product	06/20/2017
2	NDC: 71513-059-03	60 mL in 1 POUCH; Type 0: Not a Combination Product	06/20/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/20/2017

Labeler - Broder Bros Co., (005381652)

Registrant - Broder Bros Co., (005381652)

Establishment
Name	Address	ID/FEI	Business Operations
Prime Resources Corp		099761066	relabel(71513-059) , repack(71513-059)

Establishment
Name	Address	ID/FEI	Business Operations
Yuyao Jessie Commodity Co., Ltd.		529892305	manufacture(71513-059)