PowerHouse

Manufacturer
Delta Brands Inc
Effective date
2019-02-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:31:50

Label at a glance#

ProductPowerHouse ULTRA DISH Antibacterial
Active ingredientCHLOROXYLENOL
Label structure10 sections

Dosage and administration

■ wet hands ■ apply palmful to hands ■ scrub thoroughly ■ rinse thoroughly

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.30%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only: hands only

When using this product

OTC - WHEN USING SECTION

■ do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ irritation and redness develops ■ condition persists for more than 72 hours

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

■ wet hands ■ apply palmful to hands ■ scrub thoroughly ■ rinse thoroughly

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium Laureth Sulfate, Lauramine Oxide,Sodium Lauryl Sulfate, Alcohol Denat. Sodium Chloride, Tetrasodium EDTA, Fragrance, Methylchloroisothiazolinone, Methylisothiazolinone, Yellow 5, Red 40

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
20276-153-252021-07-23C16284748780-1c7ccaba7-27ed-fd44-e053-dadaa90aa01bDrug Facts

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
20276-153POWERHOUSE ULTRA DISH ANTIBACTERIAL (CHLOROXYLENOL) LIQUID [DELTA BRANDS INC]1Legacy NDC20190205_811a2587-97e8-933a-e053-2991aa0a7e5d.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
20276-15320276-153-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

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
811a2587-97ec-933a-e053-2991aa0a7e5d811a2587-97e8-933a-e053-2991aa0a7e5d2019-02-04WarningsExact identifier
spl id: 811a2587-97ec-933a-e053-2991aa0a7e5d
spl set id: 811a2587-97e8-933a-e053-2991aa0a7e5d

Reported adverse events (FAERS/openFDA)#

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