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Feminine Anti Itch Cream Benzocaine,Resorcinol 20 g/100g; 3 g/100g Cream, 3 tubes — NDC 69396-0183-33 package photo

Feminine Anti Itch Cream Benzocaine,Resorcinol 20 g/100g; 3 g/100g Cream, 3 tubes

by TRIFECTA PHARMACEUTICALS USA LLC · 3 TUBE in 1 BOX (69396-183-33) / 28.4 g in 1 TUBE
NDC 69396-0183-33
🏷️ FDA NDC (as labeled) 69396-183-33 billing pads the product segment with a zero
This package
Contains3 tubes Pack sizes2 compare ↓
Also comes in: 28.4 g 69396-0183-01
OTC On market Non-controlled
🗂️ Data synced 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

🆔 Identity & classification

FDA NDC (as labeled) 69396-183-33
Product NDC 69396-183
11-digit billing NDC 69396018333
RxCUI 637518
UNII U3RSY48JW5, YUL4LO94HK
UPC 0040232381461, 0850026393682
Application # M017
SPL Set ID 50c3acbf-b873-908a-e063-6294a90a66b7
Established class (EPC) Standardized Chemical Allergen
Physiologic effect Increased Histamine Release; Cell-mediated Immunity
Chemical class Allergens
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-04-30
Route TOPICAL
Dosage form CREAM
Substance BENZOCAINE; RESORCINOL
Why two NDCs? The FDA registers this code as 69396-183-33 — 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 → 69396-0183-33. 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 Standardized Chemical Allergen class.

Pharmacologic class Standardized Chemical Allergen
Drug family (ATC) Local anesthetics, Anesthetics for topical use, Esters of aminobenzoic acid
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.

🏭 Manufacturer & labeler

LabelerTRIFECTA PHARMACEUTICALS USA LLC
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code69396
First marketedApr 2026
Product typeHuman Otc Drug
Portfolio67 products on file
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.

🩺 Clinical

🧪 What is this product?

This is an over-the-counter topical cream marketed under FDA's OTC monograph rules for feminine anti-itch products. It contains benzocaine, a numbing agent that reduces itching and discomfort by desensitizing nerve endings in the skin, and resorcinol, which functions as a keratolytic and antimicrobial ingredient commonly used in products aimed at skin irritation and itching. The cream is applied directly to the affected area of skin to provide temporary relief from itching.

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.

🧪 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 8Z5ZAL5H3V
    A synthetic polymer made from acrylate compounds. It acts as a thickener and stabilizer in topical formulations, helping create the right texture and prevent separation of ingredients.
  • UNII RUE8E6T4NB
    Aloe vera leaf juice is a clear gel extracted from aloe vera plant leaves. It's used in medicines as a lubricant, emollient, and preservative to soothe skin contact and help keep the product stable.
  • 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 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 1C6V77QF41
    Cholecalciferol is vitamin D3, a fat-soluble vitamin added to medicines as a nutritional supplement or active ingredient fortification. It helps the body absorb calcium and support bone health.
  • 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 0RE8K4LNJS
    Isopropyl myristate is an oily liquid made from coconut or palm oil. It's used in medicines as an emollient and penetration enhancer to help the medicine absorb through skin or improve spreadability in topical products.
  • UNII 8CRQ2TH63M
    Isopropyl palmitate is an oily liquid derived from palm oil. It acts as an emollient and lubricant in medicines, helping soften the skin or improve how the product spreads and flows.
  • UNII 7EV65EAW6H
    Lanolin is a waxy substance derived from sheep's wool. It's used in medicines as an emollient and skin-conditioning agent to soften formulations and improve spreadability in topical products like creams and ointments.
  • UNII A2I8C7HI9T
    Methylparaben is a preservative derived from benzoic acid that prevents growth of bacteria, fungi, and mold in medicines. It extends the product's shelf life and maintains safety during storage.
  • 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 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 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 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 0YPR65R21J
    Sodium sulfate is a mineral salt used in pharmaceuticals as a filler and diluent. It helps provide bulk and stability to tablets and capsules while remaining inert in the body.
  • UNII K3E0U7O8KI
    A sodium salt compound used as a chelating agent and preservative in medicines. It binds to metal ions that could otherwise degrade the product, helping maintain stability and extend shelf life.
  • 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.
  • UNII 8470G57WFM
    Corn oil is a vegetable oil extracted from corn kernels. It's used in medicines as a solvent to dissolve active ingredients and help the body absorb them, and sometimes as a lubricant in capsules.

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

The official label also statesInactive ingredient Acrylates (C-10-30)alkyl acrylate crosspolymer, Aloe barbadensis leaf juice, aminomethyl propanol, cetyl alcohol, Glyceryl stearate, Isopropyl myristate, isopropyl palmitate, lanolin, methylparaben, PEG-100 stearate, Potassium cetyl phosphate, Propylene glycol, Retinyl palmitate, sdium sulfite, tocopheryl acetate, Trisodium HEDTA, vitamin D3, water, Zea mays (corn) oil.

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.

💲 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: 28.4 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Anti-Itch Medicated Maximum Strength 200 mg/g; 30 mg/g 00363-2311-28 Walgreens 1 tube — — FDA listed —
VAGISIL Anti-Itch Medicated Creme Maximum Strength 200 mg/g; 30 mg/g 11509-4402-01 Combe 1 tube — — FDA listed —
Family Wellness 20 g/100g; 3 g/100g 55621-0016-01 Zhejiang 1 tube — — FDA listed —
Feminine Anti-Itch Creme 5.67 g/28g; .85 g/28g 63868-0949-01 Quality 28 g — — FDA listed —
Feminine Anti Itch Cream 20 g/100g; 3 g/100gthis 69396-0183-33 TRIFECTA 3 tubes — — FDA listed —
HealthWise Feminine Anti-itch Cream 5.67 g/28g; .85 g/28g 71101-0035-01 Veridian 28 g — — FDA listed —
Caring Mills Vaginal Anti-Itch Cream 5.6 g/28g; .84 g/28g 71101-0039-01 Veridian 28.3 g — — FDA listed —
HealthWise Feminine Anti-Itch Cream 5.67 g/28g; .85 g/28g 71101-0049-01 Veridian 28 g — — FDA listed —
Caring Mills Vaginal Anti-Itch Cream 20 g/100g; 3 g/100g 71101-0065-01 Veridian 28.3 g — — FDA listed —
HealthWise Feminine Anti-itch Cream 20 g/100g; 3 g/100g 71101-0066-01 Veridian 28.3 g — — FDA listed —
Meijer Vagicaine 200 mg/g; 30 mg/g 79481-0130-01 Meijer, 1 tube — — FDA listed —
Equate Vagicaine 200 mg/g; 30 mg/g 79903-0233-01 Walmart 1 tube — — FDA listed —
Thera Plus Maximum Strength Feminine Anti-Itch 200 mg/g; 30 mg/g 80684-0142-00 FOURSTAR 28 g — — FDA listed —
Maximum OTC Strength Feminine Anti-Itch Creme 5.67 g/28g; .85 g/28g 83324-0019-01 Quality 28.3 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

🏛️
2026
On the market since
Apr 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
69396-0183-01 1 TUBE in 1 BOX (69396-183-01) / 28.4 g in 1 TUBE 2026-05-01 Active
69396-0183-33 You're viewing this 3 TUBE in 1 BOX (69396-183-33) / 28.4 g in 1 TUBE 2026-05-01 Active

Pack size FAQ

What quantity is in NDC 69396-0183-33?
NDC 69396-0183-33 contains 3 tubes — 3 tube in 1 box / 28.4 g in 1 tube.
What is the difference between NDC 69396-0183-33 and NDC 69396-0183-01?
Both are Feminine Anti Itch Cream Benzocaine,Resorcinol 20 g/100g; 3 g/100g Cream — the drug itself is identical. NDC 69396-0183-33 is the 3 tubes package, while NDC 69396-0183-01 is the 1 tube package.
What NDC number is used to bill for this package of Feminine Anti Itch Cream Benzocaine,Resorcinol 20 g/100g; 3 g/100g Cream?
Bill NDC 69396-0183-33 — the 11-digit billing format is 69396018333. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 FDA registers it as 69396-183-33, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 69396-0183-33, written without dashes as 69396018333. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 69396-0183-33, the first segment (69396) is the labeler code FDA assigned to TRIFECTA PHARMACEUTICALS USA LLC; the middle segment (0183) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (33) identifies this exact package size and type. Together they name one specific package of one specific product.
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 TRIFECTA PHARMACEUTICALS USA 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 1 other package presentation of this same product, including 1 tube (69396-0183-01). 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?
TRIFECTA PHARMACEUTICALS USA 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.

📄 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
🎯 Indications and Usage 4 words ▾

Uses Temporarily relieves itching.

⏱️ Dosage and Administration 43 words ▾

Directions Adults and children 12 years and older Apply a fingertip amount, approximately 1 inch strip to affected area not more than 3 to 4 times daily. Clean nozzle of tube by wiping thoroughly before replacing cap. Keep cap tightly closed between uses.

⚠️ Warnings 11 words ▾

Warning For External Use Only When using avoid contact with eyes.

🧪 Active Ingredient 6 words ▾

Active ingredients Benzocaine 20% Resorcinol 3%

🧪 Inactive Ingredients 46 words ▾

Inactive Ingredients Inactive ingredient Acrylates (C-10-30)alkyl acrylate crosspolymer, Aloe barbadensis leaf juice, aminomethyl propanol, cetyl alcohol, Glyceryl stearate, Isopropyl myristate, isopropyl palmitate, lanolin, methylparaben, PEG-100 stearate, Potassium cetyl phosphate, Propylene glycol, Retinyl palmitate, sdium sulfite, tocopheryl acetate, Trisodium HEDTA, vitamin D3, water, Zea mays (corn) oil.

🎯 Purpose 3 words ▾

Purpose External Analgesic

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 69396-0181-01 · Trifecta 69396-0184-01 · Trifecta →
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.