FDA.reportPublic FDA data

Neptune 362 Antibacterial

Manufacturer
R.L. Williams Company
Effective date
2021-01-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:44:52

Label at a glance#

ProductNeptune 362 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

Water, Sodium Laureth Sulfate, Cocoamide MEA, Sodium Lauryl Sulfate, Propylene Glycol, Glycol Stearate, Tetrasodium EDTA, Salt, Citric Acid, Methylchloroisothiazolinone, Methyl Isothiazolinone, Magnesium Chloride, Magnesium Nitrate

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
23590-11023590-110-90

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM CHLORIDE451W47IQ8XIACT
GLYCOL STEARATE0324G66D0EIACT
SODIUM LAURYL SULFATE368GB5141JIACT
EDETATE SODIUMMP1J8420LUIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
WATER059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
COCO DIETHANOLAMIDE92005F972DIACT
CHLOROXYLENOL0F32U78V2QACTIB
METHYLISOTHIAZOLINONE229D0E1QFAIACT
MAGNESIUM CHLORIDE02F3473H9OIACT
MAGNESIUM NITRATE77CBG3UN78IACT

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
e354f89e-6ba8-6da1-e053-2995a90a0fe4c24f3583-2b25-dc79-e053-2995a90a58472022-07-08WarningsExact identifier
spl set id: c24f3583-2b25-dc79-e053-2995a90a5847

Reported adverse events (FAERS/openFDA)#

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