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Verdibliss HEMORRHOID RELIEF OINTMENTS LIDOCAINE, PHENYLEPHRINE .0025 g/g; .05 g/g Ointment, 42.5 g — NDC 76986-0034-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Verdibliss HEMORRHOID RELIEF OINTMENTS LIDOCAINE, PHENYLEPHRINE .0025 g/g; .05 g/g Ointment, 42.5 g — NDC 76986-034-01 (Billing 76986-0034-01)

by Guangdong Quadrant Ecological Technology Co., Ltd. · 42.5 g in 1 BOTTLE

This is a package of 42.5 g of Verdibliss HEMORRHOID RELIEF OINTMENTS LIDOCAINE, PHENYLEPHRINE .0025 g/g; .05 g/g Ointment from Guangdong Quadrant Ecological Technology Co., Ltd., marketed since Apr 2026 and currently FDA-listed. It is this product's only package size.

NDC 76986-0034-01
🏷️ FDA NDC (as labeled) 76986-034-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Aug 27, 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 76986-034-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
76986 labeler · 034 product · 01 package
Package marketed since
Apr 10, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 7698603401 9
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 76986-034-01
Product NDC 76986-034
11-digit billing NDC 76986003401
RxCUI 2672354
UNII 1WS297W6MV, 98PI200987
Application # M015
SPL Set ID 4f1634d5-7667-b354-e063-6394a90a34e7
Established class (EPC) alpha-1 Adrenergic Agonist; Amide Local Anesthetic; Antiarrhythmic
Mechanism of action Adrenergic alpha1-Agonists
Physiologic effect Local Anesthesia
Chemical class Amides
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-04-10
Route RECTAL
Dosage form OINTMENT
Substance PHENYLEPHRINE; LIDOCAINE
Quick answers
  • RxCUI (RxNorm): 2672354
Why two NDCs? The FDA registers this code as 76986-034-01 — 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 → 76986-0034-01. 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.

RxNorm drug class

This medicine belongs to the Antiarrhythmic class.

Pharmacologic class Antiarrhythmic, Amide Local Anesthetic
Drug family (ATC) Antiarrhythmics, class Ib, Local anesthetics, Anesthetics for topical use
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?

Verdibliss Hemorrhoid Relief is a rectal ointment sold as an over-the-counter monograph product containing lidocaine and phenylephrine. Lidocaine is a local anesthetic typically used to numb and reduce pain in the affected area. Phenylephrine is a decongestant that functions as a blood vessel constrictor, commonly used to reduce swelling and discomfort associated with hemorrhoids.

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.
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
76986-0034-01 You're viewing this Main listing 42.5 g in 1 BOTTLE 2026-04-10 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Verdibliss HEMORRHOID RELIEF OINTMENTS .0025 g/g; .05 g/gthis 76986-0034-01 Guangdong 42.5 g — — FDA listed —
Dr.Seymour Butts Hemorrhoid 5 g/100g; .25 g/100g 85248-0018-01 Jiangxi 30 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.

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 YY2HMJ9NZF
    A synthetic polymer made from acrylic compounds that forms a thick, gel-like substance. It's used as a thickener and stabilizer in topical products to create the right consistency and help ingredients stay evenly mixed.
  • 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 OZ0E5Y15PZ
    A plant extract from arnica flowers, used as a flavoring agent or fragrance component in medicines. It may also provide mild soothing properties to certain topical formulations.
  • UNII 8SKN0B0MIM
    Benzoic acid is a naturally occurring organic acid used as a preservative in medicines and foods. It helps prevent bacterial and fungal growth to extend shelf life and maintain product stability.
  • UNII LKG8494WBH
    Benzyl alcohol is a clear liquid used as a preservative and solvent in medicines. It helps prevent bacterial and fungal growth and dissolves other ingredients to create uniform liquid formulations.
  • UNII 8FA93U5T67
    A waxy substance made from plant oils that acts as an emulsifier and thickener. It helps mix oil and water components in the medicine and gives the product a smooth texture.
  • 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 CI71S98N1Z
    A mineral salt containing potassium and phosphate, used as a buffer to help maintain the medicine's pH level and stability during storage.
  • 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 2R04ONI662
    Eucalyptus oil is a fragrant liquid extracted from eucalyptus tree leaves. It's used in medicines as a flavor, scent, or soothing agent in topical products and cough preparations.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • 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 CQ4IKK1766
    A synthetic oil derived from plant-based polydecene that has been chemically saturated. It functions as a lubricant and binder in tablets and capsules to improve flow and prevent sticking during manufacturing and packaging.
  • UNII 4465L2WS4Y
    A plant extract from Japanese honeysuckle flowers used as a natural flavoring and fragrance ingredient in medicines. It may also help preserve the product and add pleasant taste or aroma.
  • 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 6UYK2W1W1E
    A natural oil extracted from olives. It acts as an emollient and lubricant in formulations, helping to soften ingredients and improve how the medicine spreads or flows.
  • UNII WV9CM0O67Z
    Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.
  • UNII 4T6H12BN9U
    Petrolatum is a purified mineral oil-based jelly derived from petroleum. In medicines, it acts as an emollient, lubricant, and moisture barrier to soften skin, reduce friction, and help prevent water loss from formulations.
  • 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 C4QT53N4MK
    Potassium lauryl phosphate is a synthetic surfactant derived from lauric acid and phosphoric acid. It helps disperse and stabilize ingredients in liquid formulations, improving how the medicine mixes and stays uniform.
  • UNII 724GKU717M
    Jojoba oil is a natural liquid wax extracted from jojoba plant seeds. It's used in medicines as an emollient and lubricant to soften and smooth the product, and sometimes as a carrier or penetration enhancer.
  • UNII NG5NG5733T
    A synthetic polymer derived from acrylic acid and taurine. It functions as a suspending agent and emulsifier, helping keep ingredients evenly distributed and preventing separation in liquid or semi-solid medicines.
  • 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 2KR89I4H1Y
    Stearyl alcohol is a waxy, fatty substance derived from natural oils or made synthetically. It acts as an emulsifier and thickener in medicines, helping mix ingredients together and give the product the right texture.
  • UNII G624N6MSBA
    A synthetic surfactant derived from coconut oil. It helps dissolve and distribute other ingredients evenly throughout the medicine, acting as an emulsifier and solubilizer in liquid formulations.
  • 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 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 TTV12P4NEE
    Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.
  • UNII SOI2LOH54Z
    Zinc oxide is a white mineral powder used in medicines as a protective barrier agent and color additive. It helps shield skin in topical products and may also serve as a filler or opacifying ingredient.

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

The official label also statesWATER STEARYL ALCOHOL ZINC OXIDE GLYCERIN MINERAL OIL STEARIC ACID CETEARETH-25 GLYCERYL STEARATE CETYL ALCOHOL DIMETHICONE ARNICA MONTANA FLOWER EXTRACT SODIUM POLYACRYLOYLDIMETHYL TAURATE HYDROGENATED POLYDECENE BENZYL ALCOHOL PANTHENOL LONICERA JAPONICA (HONEYSUCKLE) FLOWER EXTRACT TRIETHANOLAMINE PHENOXYETHANOL EUCALYPTUS GLOBULUS LEAF OIL POTASSIUM LAURYL PHOSPHATE ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER OLEA EUROPAEA (OLIVE) FRUIT OIL PETROLATUM SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL XANTHAN GUM ALOE BARBADENSIS LEAF JUICE POWDER DIPOTASSIUM PHOSPHATE TRIDECETH-10 BENZOIC ACID

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

LabelerGuangdong Quadrant Ecological Technology Co., Ltd.
FDA applicationM015 (OTC MONOGRAPH DRUG)
Labeler code76986
First marketedApr 2026
Product typeHuman Otc Drug
Portfolio35 products on file

More NDCs from Guangdong Quadrant Ecological Technology Co., Lt... labeler code 76986

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 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 16 words ▾

Temporarily relieves pain, itching, and burning. Temporarily relieves swelling associated with hemorrhoids and other anorectal disorders.

⏱️ Dosage and Administration 34 words ▾

· Cleanse and dry affected area before use. · Children under 12 years: Consult a doctor before use. · Apply up to 4 times daily. · For rectal use: lubricate and insert as directed.

⚠️ Warnings 6 words ▾

For external and/or rectal use only.

🧪 Active Ingredient 4 words ▾

LIDOCAINE 5% PHENYLEPHRINE 0.25%

🧪 Inactive Ingredients 69 words ▾

WATER STEARYL ALCOHOL ZINC OXIDE GLYCERIN MINERAL OIL STEARIC ACID CETEARETH-25 GLYCERYL STEARATE CETYL ALCOHOL DIMETHICONE ARNICA MONTANA FLOWER EXTRACT SODIUM POLYACRYLOYLDIMETHYL TAURATE HYDROGENATED POLYDECENE BENZYL ALCOHOL PANTHENOL LONICERA JAPONICA (HONEYSUCKLE) FLOWER EXTRACT TRIETHANOLAMINE PHENOXYETHANOL EUCALYPTUS GLOBULUS LEAF OIL POTASSIUM LAURYL PHOSPHATE ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER OLEA EUROPAEA (OLIVE) FRUIT OIL PETROLATUM SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL XANTHAN GUM ALOE BARBADENSIS LEAF JUICE POWDER DIPOTASSIUM PHOSPHATE TRIDECETH-10 BENZOIC ACID

🎯 Purpose 3 words ▾

Topical anesthetic Vasoconstrictor

📄 Do Not Use 17 words ▾

Do not exceed the recommended dose. Do not insert using fingers or devices other than as directed.

📄 Ask a Doctor Before Use If 44 words ▾

Ask a doctor before use if you have: Some individuals may be allergic to the ingredients in this product. Heart disease, high blood pressure,thyroid disease, or diabetes.. Difficulty urinating due to an enlarged prostate. Are taking prescription drugs for high blood pressure or depression.

📄 When Using This Product 4 words ▾

Avoid contact with eyes.

📄 Stop Use and Ask a Doctor If 33 words ▾

· if bleeding occurs, symptoms worsen, or do not improve within 7 days, or if signs of an allergic reaction develop. · if you are pregnant or breastfeeding, consult your doctor before use.

📄 Keep Out of Reach of Children 13 words ▾

If swallowed, get medical help or contact a Poison Control Center right away.

📄 Package Label / Principal Display Panel 1 words ▾

label

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

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for LIDOCAINE, PHENYLEPHRINE — the ingredient across all brands.

Top reported reactions

Haemorrhage4
Burning Sensation3
Diarrhoea2
Drug Hypersensitivity2
Fatigue2
Haemorrhoids2
Pain2

Reporter sex

0 reports
Male · 13%
Female · 87%
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 8 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

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 Guangdong Quadrant Ecological Technology Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Guangdong Quadrant Ecological Technology Co., Ltd. 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.
← 76986-0033-01 · Guangdong 76986-0035-01 · Guangdong →
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.