FDA.reportPublic FDA data

Power Play

Manufacturer
Superior Chemical Corporation | Betco corporation, Ltd. | Betco Corpo, Ltd.
Effective date
2019-04-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:26:30

Label at a glance#

ProductPower Play
Active ingredientCHLOROXYLENOL
Label structure9 sections

Label contents#

Full prescribing information#

Power Play

OTC - ACTIVE INGREDIENT SECTION

​Active Ingredient

​ ​Chloroxylenol 0.5%

Power Play

INDICATIONS & USAGE SECTION

Uses

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

Power Play

WARNINGS SECTION

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

DOSAGE & ADMINISTRATION SECTION

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 INGREDIENT SECTION

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

OTC - QUESTIONS SECTION

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

MDS information:​(800) 891-4965

Power Play

OTC - PURPOSE SECTION

Purpose

Antibacterial

Power Play

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Power Play Factory Stuff

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

76544 Powerplay label76544 Powerplay label76576-00 Factory Stuff76576-00 Factory Stuff

76544 PowerPlay

76576-00 Factory Stuff

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53125-76553125-765-04, 53125-765-76

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM LAURYL SULFATE368GB5141JIACT
COCO DIETHANOLAMIDE92005F972DIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
ALLANTOIN344S277G0ZIACT
DMDM HYDANTOINBYR0546TOWIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C RED NO. 40WZB9127XOAIACT
CHLOROXYLENOL0F32U78V2QACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
abad99a2-1f41-0f8d-e053-2a95a90aa649154098d1-1ad0-4e18-913e-2c67463b0b0b2020-07-30WarningsExact identifier
spl set id: 154098d1-1ad0-4e18-913e-2c67463b0b0b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.