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Ca-Rezz Norisc Antibacterial Skin Care Benzethonium Chloride .2 g/100g Cream, 120 g — NDC 60762-0112-04 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Ca-Rezz Norisc Antibacterial Skin Care Benzethonium Chloride .2 g/100g Cream, 120 g — NDC 60762-112-04 (Billing 60762-0112-04)

by FNC MEDICAL CORPORATION · 120 g in 1 TUBE

This is a package of 120 g of Ca-Rezz Norisc Antibacterial Skin Care Benzethonium Chloride .2 g/100g Cream from FNC MEDICAL CORPORATION, marketed since Feb 2018 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.

NDC 60762-0112-04
🏷️ FDA NDC (as labeled) 60762-112-04 billing pads the product segment with a zero
This package
Contains120 g Pack sizes2 compare ↓
Main listing for product 60762-112 · Also comes in: 275 g 60762-112-09
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 60762-112-04 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
60762 labeler · 112 product · 04 package
Package marketed since
Feb 5, 2018
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0757484113091
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 60762-112-04
Product NDC 60762-112
11-digit billing NDC 60762011204
RxCUI 1372490, 1876395
UNII PH41D05744
UPC 0757484113091
Application # M003
SPL Set ID f93c55f9-b3e1-45f6-8e0d-09e60f5b822f
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2018-02-05
Route TOPICAL
Dosage form CREAM
Substance BENZETHONIUM CHLORIDE
Quick answers
  • RxCUI (RxNorm): 1372490
Why two NDCs? The FDA registers this code as 60762-112-04 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 60762-0112-04. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

RxNorm drug class

This medicine belongs to the Antiseptics class.

Drug family (ATC) Antiseptics, Quaternary ammonium compounds
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

🧪 What is this product?

Ca-Rezz Norisc is a topical cream containing benzethonium chloride, an antimicrobial agent. This product is marketed as an over-the-counter antibacterial skin care cream under FDA's OTC monograph rules. Benzethonium chloride is typically used in topical products intended to help reduce bacteria on the skin surface. This listing represents a Category I OTC monograph drug, meaning it contains an active ingredient recognized as safe and effective for its stated use category without individual FDA approval of the specific product application.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer gPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Try another pack size: 275 g
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
60762-0112-04 You're viewing this Main listing 120 g in 1 TUBE 2018-02-05 — Active
60762-0112-09 60762-112-09 275 g in 1 TUBE 2018-02-05 — Active

You're viewing the smallest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 120 g — 120 g in 1 tube.
How does this package differ from NDC 60762-0112-09?
Both are Ca-Rezz Norisc Antibacterial Skin Care Benzethonium Chloride .2 g/100g Cream — the drug itself is identical. This page's package is the 120 g one, while NDC 60762-0112-09 is the 275 g package.
What NDC number is used to bill for this package of Ca-Rezz Norisc Antibacterial Skin Care Benzethonium Chloride .2 g/100g Cream?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Ca-Rezz Norisc Antibacterial Skin Care .2 g/100gthis 60762-0112-04 FNC 120 g — — FDA listed —
Avance Incontinence Care .2 g/100g 70936-0111-27 SMART 270 g — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2018
On the market since
Feb 2018
📍
2026
Currently FDA-listed
8 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • UNII 344S277G0Z
    Allantoin is a naturally derived compound that helps soften and soothe skin. In medicines, it works as a skin-conditioning agent and may help support wound healing and reduce irritation in topical formulations.
  • UNII KIZ4X2EHYX
    A plant extract from the aloe vera leaf, used in medicines as a moisturizing agent and skin-conditioning ingredient. It helps soften and soothe the product's texture in topical formulations.
  • UNII 936JST6JCN
    Cetyl alcohol is a waxy, fatty substance derived from plant or animal sources. It acts as an emulsifier and thickener in medicines, helping blend oil and water components and giving products a smooth, creamy texture.
  • UNII 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • UNII VS041H42XC
    Ergocalciferol is a form of vitamin D derived from plant and fungal sources. It's added to medicines and supplements to provide nutritional fortification and ensure consistent vitamin D content in the product.
  • UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • UNII 230OU9XXE4
    A waxy substance made from glycerin and stearic acid that acts as an emulsifier to blend oily and watery ingredients together. It also helps thicken and stabilize the medicine's texture.
  • UNII T5L8T28FGP
    Mineral oil is a clear, odorless liquid derived from crude oil. It acts as a lubricant and emollient in medications, helping pills slide smoothly during manufacturing and aiding moisture retention in topical products.
  • UNII YD01N1999R
    A waxy substance made from polyethylene glycol and stearic acid. It helps mix oil and water-based ingredients together and serves as an emulsifier and solubilizer in liquid and semi-solid medicines.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII 65UEH262IS
    Safflower oil is a plant-based oil extracted from safflower seeds. It's used in medicines as a solvent and carrier to help dissolve or suspend active ingredients, and sometimes as an emollient to improve texture.
  • UNII 01S2G2C1E4
    Sorbitan isostearate is an emulsifier derived from sorbitol and isostearic acid. It helps mix oil and water-based ingredients together and keeps them blended throughout the medicine's shelf life.
  • UNII 4ELV7Z65AP
    Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.
  • UNII 9O3K93S3TK
    Trolamine is an alkaline compound used as a pH buffer and emulsifier in medicines. It helps neutralize acids, stabilize formulations, and enable mixing of oil and water-based ingredients.
  • UNII 1D1K0N0VVC
    A fat-soluble form of vitamin A used as a colorant and nutritional fortification ingredient. It gives products a yellow or orange tint and increases vitamin A content in the formula.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

18 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesDEIONIZED 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.

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerFNC MEDICAL CORPORATION
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code60762
First marketedFeb 2018
Product typeHuman Otc Drug
Portfolio3 products on file

More NDCs from FNC MEDICAL CORPORATION labeler code 60762

The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 32 words ▾

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.

⏱️ Dosage and Administration 23 words ▾

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

⚠️ Warnings 18 words ▾

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

🧪 Active Ingredient 5 words ▾

ACTIVE INGREDIENT BENZETHONIUM CHLORIDE 0.2%

🧪 Inactive Ingredients 36 words ▾

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.

🎯 Purpose 2 words ▾

PURPOSE ANTIBACTERIAL

📄 Keep Out of Reach of Children 6 words ▾

KEEP OUT OF REACH OF CHILDREN.

📄 Other Information 17 words ▾

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

📄 Questions or Comments 5 words ▾

QUESTIONS/COMMENTS? PLEASE CALL (800) 440-2888

📄 Package Label / Principal Display Panel 8 words ▾

Antibacterial Skin Care_Norisc Cream_120g_LBL Antibacterial Skin Care_Norisc Cream_275g_LBL

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

About this NDC listing & data coverage

Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by FNC MEDICAL CORPORATION. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 275 g (60762-0112-09). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
FNC MEDICAL CORPORATION is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 60760-0998-60 · St. 60762-0113-08 · FNC →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.