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WowDay Hemorrhoid and Fissure Cream 3.75 g/15g; 3 g/15g; .075 g/15g Cream — NDC 87113-1008-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

WowDay Hemorrhoid and Fissure Cream 3.75 g/15g; 3 g/15g; .075 g/15g Cream — NDC 87113-1008-1 (Billing 87113-1008-01)

by WowDay LLC · 1 TUBE, WITH APPLICATOR in 1 BOX / 2 g in 1 TUBE, WITH APPLICATOR

This is a package of WowDay Hemorrhoid and Fissure Cream 3.75 g/15g; 3 g/15g; .075 g/15g Cream from WowDay LLC, marketed since Feb 2026 and currently FDA-listed. It is this product's only package size.

NDC 87113-1008-01
🏷️ FDA NDC (as labeled) 87113-1008-1 billing pads the package segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 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 87113-1008-1 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
87113 labeler · 1008 product · 1 package
Package marketed since
Feb 1, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8711310081 1
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 87113-1008-1
Product NDC 87113-1008
11-digit billing NDC 87113100801
RxCUI 2734148
UNII 101I4J0U34, PDC6A3C0OX, L7T10EIP3A
Application # M015
SPL Set ID 47ba86ad-240a-e733-e063-6394a90a24e3
Established class (EPC) Non-Standardized Chemical Allergen
Physiologic effect Increased Histamine Release; Cell-mediated Immunity; Increased IgG Production
Chemical class Allergens; Glycerol
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-02-01
Route RECTAL
Dosage form CREAM
Substance WITCH HAZEL; GLYCERIN; MENTHOL
Quick answers
  • RxCUI (RxNorm): 2734148
Why two NDCs? The FDA registers this code as 87113-1008-1 — 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 → 87113-1008-01. 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 Non-Standardized Chemical Allergen class.

Pharmacologic class Non-Standardized Chemical Allergen
Drug family (ATC) Enemas, Other drugs for constipation
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?

This is an over-the-counter rectal cream marketed under FDA's OTC monograph rules for hemorrhoid and fissure relief. It contains glycerin, which functions as a lubricant and stool softener, menthol, which is typically used for its cooling and mild numbing sensation, and witch hazel, an astringent commonly used to reduce inflammation and provide a soothing effect. The combination is intended for topical application to help manage discomfort associated with hemorrhoids and anal fissures.

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
87113-1008-01 You're viewing this Main listing 1 TUBE, WITH APPLICATOR in 1 BOX / 2 g in 1 TUBE, WITH APPLICATOR 2026-02-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
WowDay Hemorrhoid and Fissure Cream 3.75 g/15g; 3 g/15g; .075 g/15gthis 87113-1008-01 WowDay 1 tube — — 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
Feb 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 3NM3F3Y6AB
    This is a synthetic derivative related to podophyllum compounds, which are plant-derived substances. It functions as a binder and structural agent in solid dosage forms, helping hold tablet or capsule ingredients together.
  • UNII C8IYT9CR7C
    Aloe emodin is a yellow compound derived from aloe plants. In medicines, it may function as a coloring agent or contribute to the formulation's stability and appearance.
  • UNII W21O437517
    A natural substance extracted from aloe vera leaves, used as a thickener and emulsifier to improve texture and help mix oil and water-based ingredients in the medicine.
  • UNII 0A5MM307FC
    A synthetic polymer that absorbs water and forms a thick, gel-like substance. In medicines, it works as a thickener and stabilizer to improve texture and help ingredients stay mixed together in creams, gels, and lotions.
  • UNII 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • UNII SML2Y3J35T
    Colchicine is an alkaloid compound derived from the autumn crocus plant. In medications, it acts as the active therapeutic ingredient rather than an inactive excipient, so it would not typically appear listed as a separate excipient on a drug label.
  • UNII 87MLH50B7Q
    A waxy steroid compound derived from cholesterol, used as a skin-conditioning agent and emollient in topical formulations to help soften and smooth the product's texture and application.
  • UNII 14255EXE39
    Ethylparaben is a preservative, a chemical that stops bacteria and mold from growing in the medicine. It keeps the product safe and effective throughout its shelf life.
  • UNII 36W3E5TAMG
    Glucomannan is a natural soluble fiber derived from the konjac plant. In medications, it acts as a binder and bulking agent, helping hold ingredients together and add volume to the formulation.
  • UNII 80ARS2076G
    A compound derived from licorice root that acts as a flavoring agent and natural sweetener. It may also help stabilize the medicine and improve its taste in oral formulations.
  • UNII GFD7C86Q1W
    A natural oil extracted from citrus peels, (+)-limonene is used as a flavoring agent and solvent in medicines. It helps dissolve active ingredients and provides a lemon or orange taste.
  • UNII WC8O09V84K
    A cooling compound made from menthol and propylene glycol carbonate. It's used in medicines for its refreshing flavor and cooling sensation, and may help deliver the active ingredient more effectively in topical or oral products.
  • UNII Z46B1LUI5N
    Mimosine is a naturally occurring amino acid compound extracted from legume plants. In medications, it serves as a buffering or pH-adjusting agent to help stabilize the formulation and maintain proper acidity levels.
  • 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 81G40H8B0T
    Vitamin A is a fat-soluble nutrient that acts as a colorant and antioxidant in medications. It prevents oxidation of other ingredients and may add nutritional value to the formulation.
  • UNII O03S90U1F2
    A synthetic compound combining vitamin E with polyethylene glycol and succinic acid. It acts as a solubilizer and antioxidant in medicines, helping dissolve poorly water-soluble drugs and prevent degradation of active ingredients.
  • UNII Y2RU654EXB
    A protein naturally made in the body that helps control blood clotting. In medicines, it's used as an active therapeutic ingredient to treat or prevent certain clotting disorders, not as an inactive filler or stabilizer.

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

The official label also statesVitamin A、 C、E, Citric Acid Monohydrate, Isoglycyrrhizinic acid, Mimosine, Epidihydrocholesterin, Colchicine, Mineral Oil, Glucomannan, Aloe-emodin, 4'-Demethylepipodofilox Benzylidene Glycoside, Aloe Vera Leaf Polysaccharides, Limonene, Carbomer, Menthol Propylene Glycol Carbonate, Ethylparaben

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

LabelerWowDay LLC
FDA applicationM015 (OTC MONOGRAPH DRUG)
Labeler code87113
First marketedFeb 2026
Product typeHuman Otc Drug
Portfolio2 products on file

More NDCs from WowDay LLC labeler code 87113

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 📄 Ask a Doctor Before Use If 📄 Ask a Doctor or Pharmacist Before Use If 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 43 words ▾

temporarily shrinks hemorrhoidal tissue temporarily relieves pain, soreness, or burning helps relieve the local itching and discomfort associated with hemorrhoids temporarily provides a coating for relief of anorectal discomforts temporarily protects the inflamed, irritated anorectal surface to help make bowel movements less painful

⏱️ Dosage and Administration 93 words ▾

cleanse the affected area with mild soap and warm water, rinse thoroughly, and then gently dry (patting or blotting) with tissue or soft cloth for application in the lower anal canal: remove cover from dispensing cap, attach dispensing cap to tube, lubricate well, then gently insert dispensing cap partway into the anus thoroughly cleanse dispensing cap after each use and replace cover children under 12 years of age consult your pediatrician adults: apply to the affected area up to 4 times daily, especially at night, in the morning or after each bowel movement

⚠️ Warnings 30 words ▾

for external use only when using finger cots or an applicator, apply externally or to the skin of the anal canal only do not put this product into the rectum

🧪 Active Ingredient 13 words ▾

Witch Hazel (25%) ……… Astringent Menthol (0.5%) …………. Analgesic Glycerin (20%) …………… Protectant

🧪 Inactive Ingredients 29 words ▾

Vitamin A、 C、E, Citric Acid Monohydrate, Isoglycyrrhizinic acid, Mimosine, Epidihydrocholesterin, Colchicine, Mineral Oil, Glucomannan, Aloe-emodin, 4'-Demethylepipodofilox Benzylidene Glycoside, Aloe Vera Leaf Polysaccharides, Limonene, Carbomer, Menthol Propylene Glycol Carbonate, Ethylparaben

🎯 Purpose 43 words ▾

temporarily shrinks hemorrhoidal tissue temporarily relieves pain, soreness, or burning helps relieve the local itching and discomfort associated with hemorrhoids temporarily provides a coating for relief of anorectal discomforts temporarily protects the inflamed, irritated anorectal surface to help make bowel movements less painful

📄 Ask a Doctor Before Use If 41 words ▾

Ask a doctor before use if you have * heart disease * diabetes * thyroid disease * high blood pressure * difficulty in urination due to enlargement of the prostate gland * allergies to any of the components of this product

📄 Ask a Doctor or Pharmacist Before Use If 24 words ▾

Ask a doctor/pharmacist before use if you are * presently taking a prescription drug for high blood pressure or depression * pregnant or breast-feeding

📄 Stop Use and Ask a Doctor If 45 words ▾

Stop use and ask a doctor if * bleeding occurs * an allergic reaction develops * condition worsens or does not improve within seven days * the symptom being treated does not subside or if redness, iritation, swelling, pain or other symptoms develop or increase

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Questions or Comments 5 words ▾

Questions or comments? Email: [email protected]

📄 Package Label / Principal Display Panel 4 words ▾

Package front Package Back

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 WowDay LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
WowDay 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.
← 87113-1001-01 · WowDay 87114-0371-36 · Zhongbaokang →
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.