NEPTUNE E2 ANTISEPTIC HAND- chloroxylenol soap 
R. L. Williams Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Soap Pro Neptune E2 ANTISEPTIC LOTION HAND SOAP

Soap Pro Neptune E2 ANTISEPTIC LOTION HAND SOAP


Active ingredient

Chloroxylenol 0.6%

Purpose

Antimicrobial

Uses

Warnings

For external use only

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

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

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

Directions

Inactive ingredients

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

Soap Pro Neptune E2 ANTISEPTIC LOTION HAND SOAP 30.4oz/900ml

NeptuneLotionHandSoapLabel

NEPTUNE E2 ANTISEPTIC HAND 
benzalkonium chloride soap
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:61159-001
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 6 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
COCO MONOETHANOLAMIDE (UNII: C80684146D)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
GLYCOL STEARATE (UNII: 0324G66D0E)  
EDETATE SODIUM (UNII: MP1J8420LU)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:61159-001-00 900 mL in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 11/14/2013
Labeler - R. L. Williams Company (099976362)
Establishment
Name Address ID/FEI Business Operations
Formula Corp. 040509648 manufacture(61159-001)

Revised: 11/2013
Document Id: bd1b9654-4da4-4f9a-ab45-f6b08893be92
Set id: ad887ee7-5a2c-4070-b8b2-d6e409ffd8c6
Version: 1
Effective Time: 20131114
 
R. L. Williams Company