CA-REZZ - NORISC - INCONTINENT WASH- benzethonium chloride solution 
FNC MEDICAL CORPORATION

----------

FNC - CA-REZZ - NORISC - INCONTINENT WASH (60762-113)

ACTIVE INGREDIENT

BENZETHONIUM CHLORIDE 0.12%

PURPOSE

ANTIBACTERIAL

USES

CA-REZZ NORSIC WASH HAS BEEN FORMULATED AS AN INCONTINENT WASH TO QUICKLY EMULSIFY BODY WASTE EVEN IN THE MOST SENSITIVE PERINEAL AREAS.

CA-REZZ NORSIC WASH IS PH BALANCED AND ENRICHED WITH ALOE VERA, TO SOOTHE AND HELP PROMOTE HEALING OF FRAGILE, IRRITATED SKIN. STOPS ODORS.

WARNINGS

FOR EXTERNAL USE ONLY. IF RASH OR IRRITATION DEVELOP, DISCONTINUE USE. CONSULT A PHYSICIAN IF IRRITATION PERSISTS.

KEEP OUT OF REACH OF CHILDREN.

DIRECTIONS

  1. SPRAY CA-REZZ NORSIC WASH WHERE URINE, FECES OR EMESIS HAS SOILED SKIN PAD LINENS AND CLOTHING.
  2. REMOVE BULK OF FECES OR EMESIS.
  3. SPRAY ADDITIONAL CA-REZZ NORSIC WASH ON WARM WET CLOTH. CLEANSE SKIN OF ALL REMAINING RESIDUE. PAT DRY. NOTE: IF AREA NEEDING CARE IS SIZEABLE AND FECAL OR EMESIS MATERIAL MASSIVE, RINSING IS ADVISED.
  4. ADD ONE CAPFUL OF CA-REZZ NORSIC WASH TO THE REGULAR LAUNDRY TO ELIMINATE RESIDUAL ODORS.

OTHER INFORMATION

CA-REZZ NORSIC WASH IS ENRICHED WITH ALOE.

INGREDIENTS

DEIONIZED WATER, SODIUM LAURETH SULFATE, PROPYLENE GLYCOL, DISODIUM COCOAMPHODIACETATE, POLYSORBATE 80 (AND) CETYL ALCOHOL (AND) ACETYLATED LANOLIN ALCOHOL, ALOE VERA EXTRACT, CITRIC ACID, PHENOXYETHANOL, ETHYHEXYLGLYCERIN, D&C YELLOW #10, FRAGRANCE.

QUESTIONS OR COMMENTS?

PLEASE CALL 1-800-440-2888

Incontinent Wash_8oz_LBL

CA-REZZ - NORISC - INCONTINENT WASH 
benzethonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60762-113
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE0.12 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
CETYL ACETATE (UNII: 4Q43814HXS)  
ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P)  
ALOE VERA WHOLE (UNII: KIZ4X2EHYX)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:60762-113-08237 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product02/05/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00302/05/2018
Labeler - FNC MEDICAL CORPORATION (849207519)

Revised: 10/2023
Document Id: 06d8b1c1-16a9-e93a-e063-6294a90a8335
Set id: ed26fa74-5ae8-4294-b61d-682d6ad4b32a
Version: 4
Effective Time: 20231003
 
FNC MEDICAL CORPORATION