POWER PLAY- chloroxylenol soap

Power Play by

Drug Labeling and Warnings

Power Play by is a Otc medication manufactured, distributed, or labeled by Superior Chemical Corporation, Betco corporation, Ltd., Betco Corpo, Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Power Play

​Active Ingredient

​ ​Chloroxylenol 0.5%

Power Play

Uses

• ​​Antibacterial hand cleaner.
• Use in daycare, hospitals, nursing homes, physicians offices, dental offices and clinics

Power Play

Warnings

• For external use only.
• Avoid contact with eyes.
• Children under the age of 6 should be supervised by an adult when using this product.
• Discontinue use is irritation or redness develops.
• If irritation persists for more than 72 hours, consult a physician.
• KEEP OUT OF REACH OF CHILDREN.

Power Play

Directions

• ​Read the entire label before using this product.
• ​Dispense 1-2 pumps of product onto wet palm.
• Lather and rinse hands with clean water

Power Play

Inactive Ingredients

​Water, Sodium Lauryl lSulfate, Coco Diethanolimide, Cocamidopropyl Betaine, Phenoxyethanol, Sodium Laureth Sulfate, Allantoin, DMDM Hydantoin, Fragrance, Aloe Barbadensis Leaf Juice, Glycerine, FD&C Yellow #5, FD&C Red #40.

Power Play

Questions or Comments?Phone: (800) 777-9343

MDS information:​(800) 891-4965

Power Play

Purpose

Antibacterial

Power Play

KEEP OUT OF REACH OF CHILDREN

Power Play Factory Stuff

76544 PowerPlay

76576-00 Factory Stuff

INGREDIENTS AND APPEARANCE

POWER PLAY 
chloroxylenol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53125-765
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
COCO DIETHANOLAMIDE (UNII: 92005F972D)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
ALLANTOIN (UNII: 344S277G0Z)
DMDM HYDANTOIN (UNII: BYR0546TOW)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 40 (UNII: WZB9127XOA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53125-765-04	3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/12/2012
2	NDC: 53125-765-76	2500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/12/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	11/12/2012

Labeler - Superior Chemical Corporation (023335086)

Registrant - Betco corporation, Ltd. (005050158)

Establishment
Name	Address	ID/FEI	Business Operations
Betco Corpo, Ltd.		005050158	manufacture(53125-765)