Home › NDC Lookup › Ingredients › Petrolatum, Zinc Oxide › 68511-0997-01
Ma Ying Long Musk Hemorrhoids PETROLATUM, ZINC OXIDE 779.9 mg/g; 76 mg/g Ointment — NDC 68511-0997-01 package photo

Ma Ying Long Musk Hemorrhoids PETROLATUM, ZINC OXIDE 779.9 mg/g; 76 mg/g Ointment

by Mayinglong Pharmaceutical Group Co., Ltd. · 1 TUBE in 1 BOX (68511-997-01) / 10 g in 1 TUBE
NDC 68511-0997-01
🏷️ FDA NDC (as labeled) 68511-997-01 billing pads the product segment with a zero
This package
Contains10 g in 1 tube Pack sizes3 compare ↓
Also comes in: 10 g 68511-0997-02 20 g 68511-0997-20
OTC On market Non-controlled
🗂️ Data synced Sep 10, 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) 68511-997-01
Product NDC 68511-997
11-digit billing NDC 68511099701
RxCUI 2396041
UNII 4T6H12BN9U, SOI2LOH54Z
UPC 0040232381232, 0850058161082
Application # M015
SPL Set ID af466f21-c4bc-3b89-e053-2995a90a49f2
Established class (EPC) Copper Absorption Inhibitor
Physiologic effect Decreased Copper Ion Absorption
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2003-12-15
Route TOPICAL
Dosage form OINTMENT
Substance PETROLATUM; ZINC OXIDE
Why two NDCs? The FDA registers this code as 68511-997-01 — 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 → 68511-0997-01. 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.

🏭 Manufacturer & labeler

LabelerMayinglong Pharmaceutical Group Co., Ltd.
FDA applicationM015 (OTC MONOGRAPH DRUG)
Labeler code68511
First marketedDec 2003
Product typeHuman Otc Drug
Portfolio2 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 ointment marketed under FDA's OTC monograph rules for hemorrhoid care. It contains petrolatum, a moisturizing emollient, and zinc oxide, a protectant commonly used in products applied to irritated skin. Together, these ingredients are typically used to soothe discomfort and protect the affected area.

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 70J9Z0J26P
    A natural resin from tree sap, amber is used as a colorant and flavor component in some medicines. It gives products a warm, golden appearance and mild aromatic qualities.
  • UNII RFM9X3LJ49
    A yellow-orange pigment produced naturally during the breakdown of hemoglobin in the body. In medicines, bilirubin may be used as a colorant or to help standardize pharmaceutical formulations for research or diagnostic purposes.
  • UNII M89NIB437X
    Borneol is a waxy, plant-derived alcohol obtained from camphor trees or made synthetically. It's used in medicines as a flavoring agent and penetration enhancer to improve how active ingredients are absorbed.
  • UNII ET3651ZLOU
    Bos taurus bile is a natural substance from cattle that contains bile acids and salts. In medicines, it helps dissolve and absorb fats and fat-soluble ingredients, and may improve how the body breaks down certain drugs.
  • UNII 97C5T2UQ7J
    Cholesterol is a fatty substance found naturally in animal tissues. In medications, it's used as an ingredient in liposomal formulations and lipid-based drug delivery systems to help encapsulate and stabilize active drugs for better absorption.
  • UNII G1JO7801AE
    Cholic acid is a naturally occurring bile acid derived from cholesterol. In medications, it acts as a solubilizer and absorption enhancer, helping dissolve and improve the body's uptake of poorly soluble drugs.
  • UNII 005990WHZZ
    A naturally occurring bile acid derived from cholesterol that helps dissolve and absorb fats and fat-soluble ingredients. In medications, it acts as a solubilizer and emulsifier to improve how the body takes in active ingredients.
  • UNII YOW8V9698H
    Dimethyl sulfoxide is a clear liquid solvent derived from wood pulp. In medicines, it helps dissolve or carry active ingredients and improve how the body absorbs the drug.
  • 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 UPS3C6CV36
    Muscone is a fragrant organic compound derived from musk deer glands or synthesized in laboratories. It is used in medicines as a fragrance and flavor ingredient to improve taste and smell.
  • UNII A75L5FZ40U
    A natural colorant derived from freshwater pearl shells. It's used to give tablets and capsules a white or iridescent appearance and shine.
  • UNII 91MBZ8H3QO
    Sodium borate is an inorganic salt compound used in medicines as a buffer to help maintain a stable pH level, and sometimes as a mild preservative or cleansing agent in topical formulations.
  • UNII 1EQV5MLY3D
    Taurine is a naturally occurring amino acid compound. In medicines, it may function as a stabilizer or buffering agent to help maintain the product's chemical balance and shelf stability.

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

The official label also statesAmber, Artificial bezoar (Bos Taurus Bile, Cholic Acid, Deoxycholic Acid, Taurine, Bilirubin, Cholesterol), Artificial musk (Muscone), Borax, Borneol, Dimethyl sulfoxide, Lanolin, Pearl

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: 10 g 20 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
Ma Ying Long Musk Hemorrhoids 779.9 mg/g; 76 mg/gthis 68511-0997-01 Mayinglong 1 tube — — FDA listed —
Mayinglong Hemorrhoidal 779.9 mg/g; 76 mg/g 68511-0998-01 Mayinglong 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

🏛️
2003
On the market since
Dec 2003
📍
2026
Currently FDA-listed
23 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
68511-0997-02 1 TUBE in 1 BOX (68511-997-02) / 10 g in 1 TUBE 2022-06-22 Active
68511-0997-01 You're viewing this 1 TUBE in 1 BOX (68511-997-01) / 10 g in 1 TUBE 2003-12-15 Active
68511-0997-20 1 TUBE in 1 BOX (68511-997-20) / 20 g in 1 TUBE 2024-05-15 Active

Pack size FAQ

What quantity is in NDC 68511-0997-01?
NDC 68511-0997-01 is listed by the FDA — 1 tube in 1 box / 10 g in 1 tube.
What NDC number is used to bill for this package of Ma Ying Long Musk Hemorrhoids PETROLATUM, ZINC OXIDE 779.9 mg/g; 76 mg/g Ointment?
Bill NDC 68511-0997-01 — the 11-digit billing format is 68511099701. 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 68511-997-01, 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: 68511-0997-01, written without dashes as 68511099701. 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 68511-0997-01, the first segment (68511) is the labeler code FDA assigned to Mayinglong Pharmaceutical Group Co., Ltd.; the middle segment (0997) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 Mayinglong Pharmaceutical Group Co., Ltd.. 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 1 tube (68511-0997-02), 1 tube (68511-0997-20). 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?
Mayinglong Pharmaceutical Group 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.

📄 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 76 words ▾

Uses For the temporary relief of local itching and discomfort associated with hemorrhoids Temporarrily forms a protective coating over inflamed tissue to help prevent drying of tissues. Temporarily protects irritated areas. Temporaily relieves burning.

Provides temporary relief from skin irritation. Temporarily provides a coating for relief of anorectal discomforts. Temporarily protects the inflamed, irritated anorectal surface to help make bowel movements less painful Temporarily protects inflamed perianal skin.

Temporarily relieves the symptoms of perianal skin irritation.

⏱️ Dosage and Administration 84 words ▾

Directions Adults: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of the ointment. Apply to the affected area up to 2 times daily or after each bowel movement.

Apply liberally to the affected area. FOR INTRARECTAL USE: Attach applicator to tube. Lubricant applicator well with ointment, then gently insert applicator into the rectum Children under 12 years of age: consult a doctor.

⚠️ Warnings 121 words ▾

Warnings For external and/or intrarectal use only Do not use If allergic to any of the ingredients When using this product Do not exceed the recommended number of daily uses unless directed by a doctor. Do not use the product with an applicator if the introduction of the applicator into the rectum causes additional pain. Consult a doctor promptly.

Stop use and ask a doctor if Bleeding occurs Condition worsens or does not improve within 7 days Do not use during pregnancy or when breast-feeding, Consult a health professional before use. Keep out of reach of children to avoid accidental poisoning. If swallowed, get medical help or contact a Poison Control Center right away.

Do not use otherwise than as directed.

🧪 Active Ingredient 9 words ▾

Active Ingredients Petrolatum 77.99% Calamine 7.6% Purpose Protectant Astringent

🧪 Inactive Ingredients 24 words ▾

Inactive ingredients Amber, Artificial bezoar (Bos Taurus Bile, Cholic Acid, Deoxycholic Acid, Taurine, Bilirubin, Cholesterol), Artificial musk (Muscone), Borax, Borneol, Dimethyl sulfoxide, Lanolin, Pearl

🎯 Purpose 3 words ▾

Purpose Protectant Astringent

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 68479-0991-00 · Dermalogica, 68511-0998-01 · Mayinglong →
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.