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ReVive Fermitif Neck Renewal SPF 15 AVOBENZONE, OCTINOXATE, OCTOCRYLENE, OXYBENZONE 20 mg/mL; 60 mg/mL; 27 mg/mL; 20 mg/mL Cream, 75 mL — NDC 65342-1230-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

ReVive Fermitif Neck Renewal SPF 15 AVOBENZONE, OCTINOXATE, OCTOCRYLENE, OXYBENZONE 20 mg/mL; 60 mg/mL; 27 mg/mL; 20 mg/mL Cream, 75 mL — NDC 65342-1230-1 (Billing 65342-1230-01)

by Gurwitch Products, LLC · 75 mL in 1 JAR

This is a package of 75 mL of ReVive Fermitif Neck Renewal SPF 15 AVOBENZONE, OCTINOXATE, OCTOCRYLENE, OXYBENZONE 20 mg/mL; 60 mg/mL; 27 mg/mL; 20 mg/mL Cream from Gurwitch Products, LLC, marketed since May 2011 and currently FDA-listed. It is the main listing for this product, which comes in 3 package sizes.

NDC 65342-1230-01
🏷️ FDA NDC (as labeled) 65342-1230-1 billing pads the package segment with a zero
This package
Contains75 mL Pack sizes3 compare ↓
Main listing for product 65342-1230 · Also comes in: 15 ml 65342-1230-3 30 ml 65342-1230-2
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 65342-1230-1 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
65342 labeler · 1230 product · 1 package
Package marketed since
Dec 19, 2017
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 6534212301 6
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 65342-1230-1
Product NDC 65342-1230
11-digit billing NDC 65342123001
UNII G63QQF2NOX, 4Y5P7MUD51, 5A68WGF6WM, 95OOS7VE0Y
Application # M020
SPL Set ID de54d4ff-f9b4-4a12-95ea-fc2b61bee1c3
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2011-05-06
Route TOPICAL
Dosage form CREAM
Substance AVOBENZONE; OCTINOXATE; OCTOCRYLENE; OXYBENZONE
Why two NDCs? The FDA registers this code as 65342-1230-1 — a 5-4-1 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 package segment → 65342-1230-01. 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.

Clinical

🧪 What is this product?

ReVive Fermitif Neck Renewal SPF 15 is a topical cream containing four chemical UV filters: avobenzone, octinoxate, octocrylene, and oxybenzone. These ingredients are typically used together in sunscreen products to absorb and scatter ultraviolet rays from the sun. This product is marketed as an over-the-counter monograph drug, meaning it follows FDA's established safety and effectiveness standards for sunscreen ingredients rather than undergoing individual product review.

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: 15 ml 30 ml
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
65342-1230-01 You're viewing this Main listing 75 mL in 1 JAR 2017-12-19 — Active
65342-1230-02 65342-1230-2 30 mL in 1 JAR 2017-12-19 — Active
65342-1230-03 65342-1230-3 15 mL in 1 JAR 2017-12-19 — Active

You're viewing the largest of 3 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 75 mL — 75 ml in 1 jar.
How does this package differ from NDC 65342-1230-03?
Both are ReVive Fermitif Neck Renewal SPF 15 AVOBENZONE, OCTINOXATE, OCTOCRYLENE, OXYBENZONE 20 mg/mL; 60 mg/mL; 27 mg/mL; 20 mg/mL Cream — the drug itself is identical. This page's package is the 75 mL one, while NDC 65342-1230-03 is the 15 ml package.
What NDC number is used to bill for this package of ReVive Fermitif Neck Renewal SPF 15 AVOBENZONE, OCTINOXATE, OCTOCRYLENE, OXYBENZONE 20 mg/mL; 60 mg/mL; 27 mg/mL; 20 mg/mL 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
ReVive Fermitif Neck Renewal SPF 15 20 mg/mL; 60 mg/mL; 27 mg/mL; 20 mg/mLthis 65342-1230-01 Gurwitch 75 ml — — 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

🏛️
2011
On the market since
May 2011
📍
2026
Currently FDA-listed
15 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 ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • UNII LU49E6626Q
    A synthetic organic compound used as a pH buffer and neutralizing agent in medicines. It helps maintain the proper acidity level in liquid formulations to improve stability and comfort.
  • UNII 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • UNII 00YIU5438U
    Caprylyl glycol is a clear liquid derived from coconut oil. In medicines, it acts as a humectant to retain moisture, a preservative booster to prevent microbial growth, and a solvent to help dissolve or mix other ingredients.
  • UNII I670DAL4SZ
    A preservative that fights bacteria and fungi. It keeps medicines and topical products stable and safe from microbial contamination during storage and use.
  • UNII 9DBA0SBB0L
    A synthetic red dye derived from coal tar used as a colorant in medicines and cosmetics. It gives tablets, capsules, and liquids their red or pink appearance for identification and visual appeal.
  • 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 7FLD91C86K
    Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
  • UNII L837108USY
    Geraniol is a natural fragrant compound found in plants like roses and lemons. It's used in medicines as a flavoring agent and to improve the taste or aroma of the product.
  • UNII YSE9PPT4TH
    Hyaluronate sodium is a natural carbohydrate that holds moisture. It's used in medicines as a lubricant, thickener, and moisture-retaining agent to improve texture and delivery of the active ingredient.
  • UNII 24WE03BX2T
    Levomenol is a naturally derived alcohol compound used as a skin-conditioning and anti-inflammatory agent in topical formulations. It helps soothe and protect the skin while improving product texture and absorption.
  • UNII 6M3P64V0NC
    A fine powder made from magnesium, aluminum, and silicon compounds. It absorbs moisture and helps keep medicine ingredients from clumping or separating, so the product stays stable and flows smoothly during manufacturing.
  • 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 03KCY6P7UT
    A waxy compound derived from cetyl alcohol and phosphoric acid. It acts as an emulsifier to help blend oil and water ingredients, and as a thickener to give the medicine its proper texture and consistency.
  • UNII 07V4DX094T
    Sambucus nigra flower is an extract from the black elderflower plant. It may be added to medicines as a flavoring or coloring agent, or to provide traditional herbal characteristics to the formulation.
  • UNII 469OTG57A2
    Sodium pyrrolidone carboxylate is a synthetic polymer derived from pyrrolidone chemistry. It functions as a solubilizer and binder in medications, helping dissolve poorly water-soluble drugs and hold tablet ingredients together.
  • UNII NVZ4I0H58X
    A waxy substance made from sorbitol and stearic acid. It acts as an emulsifier and stabilizer, helping keep oil and water mixed together and preventing separation in the medicine.
  • UNII 3W1JG795YI
    Sunflower oil is a natural vegetable oil derived from sunflower seeds. It serves as a solvent, lubricant, and carrier in medicines, helping dissolve active ingredients and improve how the medication flows and absorbs in the body.
  • UNII 28F9E0DJY6
    Tannic acid is a plant-derived compound that acts as an astringent and antioxidant in medications. It's used to help bind ingredients together, preserve the product, and reduce moisture absorption in solid dosage forms.
  • 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.

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

The official label also statesINACTIVE INGREDIENTS: Water (Aqua), Helianthus Annuus (Sunflower) Seed Oil, Emulsifying Wax NF, Butylene Glycol, Squaiane, PPG-2 Myristyl Ether Propionate, Potassium Cetyl Phosphate, Isocetyl Stearate, Sorbitan Stearate, Terminalia Catappa Leaf Extract, Sambucus Nigra Flower Extract, PVP, Tannic Acid, Methylsilanol Hydroxyproline Aspartate, Hydrolyzed Soy Flour, Glycolipids, rh-Oligopeptide-1, rh-Polypeptide-1, Sodium Hyaluronate, Tocopheryl Acetate, Dimethicone, Bisabolol, Aliantoin, Aloe Barbadensis Leaf Juice, Sodium PCA, Carbomer, Magnesium Aluminum Silicate, Disodium EDTA, Aminomethyl Propanol, Phenoxyethanol, Caprylyl Glycol, Chlorphenesin, Geraniol, Citronellol, Fragrance (Parfum), Red 33 (CI 17200).

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

LabelerGurwitch Products, LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code65342
First marketedMay 2011
Product typeHuman Otc Drug
Portfolio2 products on file

More NDCs from Gurwitch Products, LLC labeler code 65342

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.
🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📋 Description 📄 When Using This Product 📄 Package Label / Principal Display Panel
🧪 Active Ingredient 10 words ▾

ACTIVE INGREDIENTS: Avobenzone (2.0%), Octinoxate (6.0%), Octocrylene (2.7%), Oxybenzone (2.0%).

🧪 Inactive Ingredients 79 words ▾

INACTIVE INGREDIENTS: Water (Aqua), Helianthus Annuus (Sunflower) Seed Oil, Emulsifying Wax NF, Butylene Glycol, Squaiane, PPG-2 Myristyl Ether Propionate, Potassium Cetyl Phosphate, Isocetyl Stearate, Sorbitan Stearate, Terminalia Catappa Leaf Extract, Sambucus Nigra Flower Extract, PVP, Tannic Acid, Methylsilanol Hydroxyproline Aspartate, Hydrolyzed Soy Flour, Glycolipids, rh-Oligopeptide-1, rh-Polypeptide-1, Sodium Hyaluronate, Tocopheryl Acetate, Dimethicone, Bisabolol, Aliantoin, Aloe Barbadensis Leaf Juice, Sodium PCA, Carbomer, Magnesium Aluminum Silicate, Disodium EDTA, Aminomethyl Propanol, Phenoxyethanol, Caprylyl Glycol, Chlorphenesin, Geraniol, Citronellol, Fragrance (Parfum), Red 33 (CI 17200).

🎯 Purpose 5 words ▾

SKIN TYPE: All skin types.

📋 Description 75 words ▾

ReVive Fermitif Neck Renewal Cream SPF 15 is a luxurious rose-infused formula designed to give the neck and decolletage - areas that are a dead giveaway to the effects of skin aging - a creamy, taut, firm appearance while protecting from the harshness of sun damage. With EGF (Epidermal Growth Factor), a bioengineered protein that dramatically increases skin cell renewal, and special firming agents. Fermitif promotes lustrous skin resistant to the daily pull of gravity.

📄 When Using This Product 17 words ▾

APPLICATION: Smooth over neck and decolletage morning and night after cleansing and toing. Follow with face products.

📄 Package Label / Principal Display Panel 36 words ▾

Re Vive FERMITIF NECK RENEWAL CREAM SPF 15 CREME POUR LE COU NET WT

2.5 FL OZ / 75 ML

Research Renewal Results. ReVive Fermitif Neck Renewal Cream SPF 15 PATENTED TECHNOLOGY.

FERMITIF A

FERMITIF B

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 Gurwitch Products, LLC. 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 2 other package presentations of this same product, including 15 ml (65342-1230-03), 30 ml (65342-1230-02). 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?
Gurwitch Products, LLC 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.
← 65326-0004-00 · Cayman 65342-2340-01 · Gurwitch →
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.