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

  • Handwash to help decrease bacteria on the skin
  • Recommended for repeated use

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

  • 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

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 TypeHUMAN OTC DRUGItem Code (Source)NDC:61159-001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL6 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61159-001-00900 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E11/14/201301/28/2016
Labeler - R. L. Williams Company (099976362)
Establishment
NameAddressID/FEIBusiness Operations
Formula Corp.040509648manufacture(61159-001)

Revised: 1/2016
 
R. L. Williams Company