Neptune 367 Foaming Antibacterial

Manufacturer: R.L. Williams Company
Effective date: 2021-01-04
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 22:44:47

Label at a glance#

ProductNeptune 367 Foaming Antibacterial

Active ingredientCHLOROXYLENOL

Label structure8 sections

Indications and uses

Uses Hand wash to decrease bacteria on the skin Recommended for repeated use.

Dosage and administration

Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands for 15 seconds. Rinse with potable water.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.3%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Uses

Hand wash to decrease bacteria on the skin
Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes. In case of contact, rinse eyes thorooughly with water.

Stop use

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. I swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Pump a small amount of foam into palm of hand.
Rub thoroughly over all surfaces of both hands for 15 seconds.
Rinse with potable water.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Sodium Laureth Sulfate, Sodium Lauryl Sulfate, Lauramide DEA, Cocamide, Cocamidopropyl Betaine, Sodium Cumenesulfonate, Propylene Glycol, Citric Acid, Aloe, Tocopheryl Acitate, Fragrance, and Water,

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Products#

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

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

Neptune 367 Foaming Antibacterial
Chloroxyenol
CHLOROXYLENOL
ALOE
ALPHA-TOCOPHEROL ACETATE
LAURIC DIETHANOLAMIDE
SODIUM CUMENESULFONATE
PROPYLENE GLYCOL
CITRIC ACID MONOHYDRATE
SODIUM LAURYL SULFATE
COCAMIDE
COCAMIDOPROPYL BETAINE
WATER
SODIUM LAURETH SULFATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
23590-120	23590-120-90

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
CHLOROXYLENOL	0F32U78V2Q	ACTIB
ALOE	V5VD430YW9	IACT
ALPHA-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
LAURIC DIETHANOLAMIDE	I29I2VHG38	IACT
SODIUM CUMENESULFONATE	5798KA13PG	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
SODIUM LAURYL SULFATE	368GB5141J	IACT
COCAMIDE	3YXD33R71G	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
WATER	059QF0KO0R	IACT
SODIUM LAURETH SULFATE	BPV390UAP0	IACT

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
e354ed4a-44c3-0dcc-e053-2a95a90a6789			c2502fa5-546d-320b-e053-2a95a90ac089	2022-07-08	Warnings	Exact identifier spl set id: c2502fa5-546d-320b-e053-2a95a90ac089

Reported adverse events (FAERS/openFDA)#

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