CA-REZZ NORISC ANTIBACTERIAL SKIN CARE

Dosage form: cream
Ingredients: BENZETHONIUM CHLORIDE 0.2g in 100g
Labeler: FNC MEDICAL CORPORATION
NDC code: 60762-112

Medically reviewed by Drugs.com. Last updated on Jan 26, 2024.

CA-REZZ - NORISC CREAM - ANTIBACTERIAL SKIN CARE

ACTIVE INGREDIENT

BENZETHONIUM CHLORIDE 0.2%

PURPOSE

ANTIBACTERIAL

USES

CA-REZZ NORSIC CREAM IS A NON-GREASY ANTIBACTERIAL CREAM SPECIALLY FORMULATED TO SOOTHE SKIN TISSUE. IT IS IDEAL FOR USE ON IRRITATED SKIN. IT REDUCES COMMON GERMS THAT CAN CAUSE PAINFUL RASHES.

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

APPLY A SMALL AMOUNT OF CREAM TO SKIN AND RUB GENTLY.
USE AS A MASSAGE CREAM FOR IMMOBILE PATIENTS TO IMPROVE CIRCULATION.

OTHER INFORMATION

CA-REZZ NORSIC CREAM IS ENRICHED WITH VITAMINS A, D & E, ALOE VERA AND ALLANTOIN.

INACTIVE INGREDIENTS

DEIONIZED WATER, MINERAL OIL, ALOE VERA EXTRACT, PROPYLENE GLYCOL, STEARIC ACID, GLYCERYL STEARATE AND PEG 100 STEARATE, SAFFLOWER OIL, CETYL ALCOHOL, TRIETHANOLAMINE, SORBITAN, ISOSTEARATE, DIMETHICONE, ALLANTOIN, TOCOPHERYL ACETATE, RETINYL PALMITATE, ERGOCALCIFEROL, PHENOXYETHANOL, ETHYLHEXYLGLYCERIN, FRAGRANCE.

QUESTIONS/COMMENTS?

PLEASE CALL (800) 440-2888

CA-REZZ NORISC ANTIBACTERIAL SKIN CARE
benzethonium chloride cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:60762-112
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (BENZETHONIUM)	BENZETHONIUM CHLORIDE	0.2 g in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER
MINERAL OIL
ALOE VERA WHOLE
PROPYLENE GLYCOL
STEARIC ACID
GLYCERYL MONOSTEARATE
PEG-100 STEARATE
SAFFLOWER OIL
CETYL ALCOHOL
TROLAMINE
SORBITAN ISOSTEARATE
DIMETHICONE
ALLANTOIN
.ALPHA.-TOCOPHEROL ACETATE
VITAMIN A PALMITATE
ERGOCALCIFEROL
PHENOXYETHANOL
ETHYLHEXYLGLYCERIN

Packaging
#	Item Code	Package Description
1	NDC:60762-112-09	275 g in 1 TUBE
2	NDC:60762-112-04	120 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/05/2018

Labeler - FNC MEDICAL CORPORATION (849207519)

Registrant - FNC MEDICAL CORPORATION (849207519)

Establishment
Name	Address	ID/FEI	Operations
FNC MEDICAL CORPORATION		849207519	label(60762-112), manufacture(60762-112)

Revised: 02/2018

Document Id: 2ced41a4-4ada-4251-bfec-9445f2b748dd

Set id: f93c55f9-b3e1-45f6-8e0d-09e60f5b822f

Version: 1

Effective Time: 20180205

FNC MEDICAL CORPORATION

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer

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