FDA.reportPublic FDA data

NorthWoods PowerPlay

Manufacturer
Northwoods PowerPlay | Betco Corp Ltd
Effective date
2025-10-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:38:18

Label at a glance#

ProductNorthWoods PowerPlay
Active ingredientCHLOROXYLENOL
Label structure9 sections

Label contents#

Full prescribing information#

doasge

DOSAGE & ADMINISTRATION SECTION

Place enough product on palms and scurb thoroughly over all surfaces of both hands

inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Lauryl Sufate, Ethylen Glycol Phenyl Ether, Cocamidopropyle Amine Oxide,Sodium Chloride, Propylene Glycol, Fragrance, Sodium Benzoate, Glycol Distearate, Lauramide MIPA, Sdoium Hydroxide, Disodium Cocamido,MIPA Sulfosuccinate, D&C Green 5, FD&C Yellow 5

instructions for use

INSTRUCTIONS FOR USE SECTION

Place enough product on your palm and scrub thoroughly over all surfaces of both hands. Rinse with Clean water

active

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol

Keep out of reach

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN. If swallowed get medical help or contact Poison Control center right away

purpose

OTC - PURPOSE SECTION

Antibacterial

warning

WARNINGS SECTION

For external use only

When using this product aboid contact with eyes

If Contact occurs rinse thoroughly wiht water

Stop use and ask a doctor if rritation or rash occurs

usage

INDICATIONS & USAGE SECTION

Antibacterial Hand Cleaner

Use in Daycare, Hospitals, Nursing Homes, physicians offices, dental offices and clinics

label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1362618chloroxylenol 0.375 % Medicated Liquid SoapPSN3
1362618chloroxylenol 3.75 MG/ML Medicated Liquid SoapSCD3
1362618chloroxylenol 0.375 % Medicated Liquid SoapSY3

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130814410022039GTIN-13: 0814410022039
EAN-13: 0814410022039
GTIN-12: 814410022039
UPC-A: 814410022039
GTIN storage (14 digits): 00814410022039		14104 PowerPlay Label-01.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53125-814-04NorthWoods PowerPlay3780 mL in 1 BOTTLE, PLASTICLIQUID37803

Products#

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

DailyMed product names page 1 of 1 · 40 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53125-81453125-814-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 39 matching rows.

Name, UNII, Kind table
NameUNIIKind
VERDYL ACETATE5232EN3X2FIACT
ETHYLENE OXIDEJJH7GNN18PIACT
SODIUM ALUMINIUM SILICATE058TS43PSMIACT
D&C GREEN NO. 58J6RDU8L9XIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
SODIUM BENZOATEOJ245FE5EUIACT
PHENOXYETHANOLHIE492ZZ3TIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
.ALPHA.-AMYLCINNAMALDEHYDEWC51CA3418IACT
BENZYL SALICYLATEWAO5MNK9TUIACT
.GAMMA.-UNDECALACTONEQB1T0AG2YLIACT
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XIACT
2-TERT-BUTYLCYCLOHEXYL ACETATE364FV60913IACT
CALCIUM SILICATES4255P4G5MIACT
LINALOOLD81QY6I88EIACT
TRIBASIC CALCIUM PHOSPHATE91D9GV0Z28IACT
COCAMIDOPROPYLAMINE OXIDEM4SL82J7HKIACT
1-(2,3,8,8-TETRAMETHYL-1,2,3,4,5,6,7,8-OCTAHYDRONAPHTHALEN-2-YL)ETHANONE1GD7ODM28YIACT
.BETA.-CITRONELLOL, (+/-)-565OK72VNFIACT
3-(3,4-METHYLENEDIOXYPHENYL)-2-METHYLPROPANALL65EG8H6PAIACT
HEXYL SALICYLATE8F78EY72YLIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ETHYLENE BRASSYLATE9A87HC7RODIACT
2,6-DIMETHYL-5-HEPTENALZ331YX9EL9IACT
LAURIC ISOPROPANOLAMIDE82DUX3RRVUIACT
SODIUM LAURYL SULFATE368GB5141JIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
4-ACETOXY-3-PENTYLTETRAHYDROPYRAN30E3255185IACT
DIHYDROMYRCENOL46L1B02ND9IACT
CHLOROXYLENOL0F32U78V2QACTIB
PHENYLETHYL ALCOHOLML9LGA7468IACT
BENZYL ACETATE0ECG3V79ZJIACT
SODIUM HYDROXIDE55X04QC32IIACT
GLYCOL DISTEARATE13W7MDN21WIACT
HEXAHYDRO-4,7-METHANOINDEN-6-YL PROPIONATES3ASM14UASIACT
SODIUM CARBONATE45P3261C7TIACT
2-ISOBUTYL-4-METHYLTETRAHYDROPYRAN-4-OLVK5ZHH2T3FIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-03-03full-release2026-06-01 00:56:32

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
NorthWoods PowerPlayCHLOROXYLENOLNorthwoods PowerPlay2e82fba4-960f-eccc-e063-6294a90a43de2025-10-08WarningsExact identifier
ndc (package): 53125-814-04
ndc (product): 53125-814
ndc11 (package): 53125081404
spl id: 40a726bd-bc29-3edb-e063-6294a90a08f2
spl set id: 2e82fba4-960f-eccc-e063-6294a90a43de

Reported adverse events (FAERS/openFDA)#

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