Antibacterial Skin Rain Forest Extract From Entiere

Manufacturer: World Club Supply Corp
Effective date: 2025-01-10
Label type: HUMAN OTC DRUG LABEL
Version: 7
Source: legacy-cache
Hydrated at: 2026-08-01 20:42:36

Label at a glance#

ProductAntibacterial Skin Rain Forest Extract From Entiere

Active ingredientCHLOROXYLENOL

Label structure7 sections

Indications and uses

for handwashing to decrease bacteria on the skin

Dosage and administration

Wash hands and rinse

Contacts and useful links#

PhoneLabel contact1-800-356-CLUB

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.25%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes. In case of eye contact, flush with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Irritation or redness develops

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

Wash hands and rinse

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water (aqua), Cocamidopropyl Betaine, Sodium Laureth Sulfate, Cocamide DIPA, Sodium Lauryl Sulfate, Sodium Chloride, Fatty Ester, Polysorbate 20, Fragrance, DMDM Hydantoin, Polyquaternium-7, Disodium EDTA, Citric Acid.

Questions?

OTC - QUESTIONS SECTION

1-800-356-CLUB (2582)

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label0

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

Antibacterial Skin Rain Forest Extract From Entiere
CHLOROXYLENOL
WATER
COCAMIDOPROPYL BETAINE
SODIUM LAURETH SULFATE
SODIUM CHLORIDE
DMDM HYDANTOIN
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW)
EDETATE DISODIUM
CITRIC ACID ACETATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
64987-0266	64987-0266-6

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
SODIUM LAURETH SULFATE	BPV390UAP0	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
DMDM HYDANTOIN	BYR0546TOW	IACT
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW)	0L414VCS5Y	IACT
EDETATE DISODIUM	7FLD91C86K	IACT
CITRIC ACID ACETATE	DSO12WL7AU	IACT
CHLOROXYLENOL	0F32U78V2Q	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
2e2750e6-4681-7dfd-e063-6394a90a4ee8			5a2dd638-8b9f-4a52-e053-2991aa0affb1	2025-02-14	Warnings	Exact identifier spl set id: 5a2dd638-8b9f-4a52-e053-2991aa0affb1

Reported adverse events (FAERS/openFDA)#

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