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Peppermint soothing cream CAMPHORIC ACID, MENTHOL, UNSPECIFIED FORM, BORNEOL 3.5 g/100g; 2 g/100g; 1 g/100g Paste — NDC 85305-0001-03 package photo

Peppermint soothing cream CAMPHORIC ACID, MENTHOL, UNSPECIFIED FORM, BORNEOL 3.5 g/100g; 2 g/100g; 1 g/100g Paste

by Henan Lijitang Medical Technology Co., Ltd. · 1 BOTTLE in 1 BOX (85305-001-03) / 100 g in 1 BOTTLE
NDC 85305-0001-03
🏷️ FDA NDC (as labeled) 85305-001-03 billing pads the product segment with a zero
This package
Contains100 g in 1 bottle Pack sizes4 compare ↓
Also comes in: 30 g 85305-0001-01 50 g 85305-0001-02 120 g 85305-0001-04
OTC On market Non-controlled
🗂️ Data synced 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

🆔 Identity & classification

FDA NDC (as labeled) 85305-001-03
Product NDC 85305-001
11-digit billing NDC 85305000103
UNII 32K0C7JGCJ, L7T10EIP3A, M89NIB437X
UPC 6971876476111
Application # M017
SPL Set ID 2f6bc332-3006-710d-e063-6394a90acea5
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-03-13
Route TOPICAL
Dosage form PASTE
Substance CAMPHORIC ACID; MENTHOL, UNSPECIFIED FORM; BORNEOL
Why two NDCs? The FDA registers this code as 85305-001-03 — 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 → 85305-0001-03. 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

LabelerHenan Lijitang Medical Technology Co., Ltd.
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code85305
First marketedMar 2025
Product typeHuman Otc Drug
Portfolio4 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?

Peppermint soothing cream is a topical paste containing menthol, camphor acid, and borneol. These ingredients are commonly used in over-the-counter products for their cooling and soothing sensations when applied to the skin. This product is marketed as an OTC monograph drug, meaning it follows FDA's established rules for this category of topical comfort products rather than being individually approved.

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 1V63N2S972
    A plant extract from angelica dahurica root used in traditional formulations. It may function as a flavoring agent, fragrance component, or natural ingredient to add therapeutic appeal to the medicine.
  • UNII B86IS274O0
    A plant extract from safflower flower buds used as a natural colorant and flavoring agent in medicines. It provides color and taste to make the product more appealing.
  • UNII C5529G5JPQ
    Ginger is a plant-derived ingredient used as a flavoring agent to add taste and aroma to medicines. It may also provide mild soothing properties to support product palatability.
  • UNII 82IL3676HG
    A plant-derived substance from Kadsura heteroclita stems, used as a natural extract or botanical ingredient. It may function as a flavor, color, or bioactive component in formulations.
  • UNII GQX1C1175U
    A plant extract from Panax notoginseng root used in traditional medicine formulations. It may function as a filler or active botanical component in herbal or dietary supplement products.
  • UNII S2ULN37C9R
    A synthetic chemical compound derived from vanillin that acts as a flavoring agent and fragrance enhancer in medicines. It provides vanilla-like taste and aroma to improve the palatability of oral medications.
  • UNII F84709P2XV
    Wormwood is a plant extract used as a flavoring agent in medicines. It provides a bitter taste to help mask other flavors or make the medication easier to take.

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

The official label also statesANGELICA DAHURICA ROOT KADSURA HETEROCLITA STEM GINGER PANAX NOTOGINSENG ROOT CARTHAMUS TINCTORIUS FLOWER BUD WORMWOOD VANILLYL BUTYL ETHER

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: 30 g 50 g 120 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
Peppermint soothing cream 3.5 g/100g; 2 g/100g; 1 g/100gthis 85305-0001-03 Henan 1 bottle — — 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

🏛️
2025
On the market since
Mar 2025
📍
2026
Currently FDA-listed
1 year 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
85305-0001-01 1 BOTTLE in 1 BOX (85305-001-01) / 30 g in 1 BOTTLE 2025-03-13 Active
85305-0001-02 1 BOTTLE in 1 BOX (85305-001-02) / 50 g in 1 BOTTLE 2025-03-13 Active
85305-0001-03 You're viewing this 1 BOTTLE in 1 BOX (85305-001-03) / 100 g in 1 BOTTLE 2025-03-13 Active
85305-0001-04 1 BOTTLE in 1 BOX (85305-001-04) / 120 g in 1 BOTTLE 2025-03-13 Active

Pack size FAQ

What quantity is in NDC 85305-0001-03?
NDC 85305-0001-03 is listed by the FDA — 1 bottle in 1 box / 100 g in 1 bottle.
What NDC number is used to bill for this package of Peppermint soothing cream CAMPHORIC ACID, MENTHOL, UNSPECIFIED FORM, BORNEOL 3.5 g/100g; 2 g/100g; 1 g/100g Paste?
Bill NDC 85305-0001-03 — the 11-digit billing format is 85305000103. 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 85305-001-03, 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: 85305-0001-03, written without dashes as 85305000103. 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 85305-0001-03, the first segment (85305) is the labeler code FDA assigned to Henan Lijitang Medical Technology Co., Ltd.; the middle segment (0001) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (03) 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 Henan Lijitang Medical Technology 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 3 other package presentations of this same product, including 1 bottle (85305-0001-01), 1 bottle (85305-0001-02), 1 bottle (85305-0001-04). 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?
Henan Lijitang Medical 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.

📄 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 9 words ▾

Specially formulated for: ARTHRITISNECK & BACK PAINMUSCULAR ACHES& PAINS

⏱️ Dosage and Administration 23 words ▾

Apply a small amount of Pain Relief Ointment tothe affected area & gently massage in untilfully absorbed.Use twice daily or morefrequently if required.

⚠️ Warnings 4 words ▾

For External use only

🧪 Active Ingredient 9 words ▾

CAMPHORIC ACID 3.5% MENTHOL, UNSPECIFIED FORM 2% BORNEOL 1%

🧪 Inactive Ingredients 18 words ▾

ANGELICA DAHURICA ROOT KADSURA HETEROCLITA STEM GINGER PANAX NOTOGINSENG ROOT CARTHAMUS TINCTORIUS FLOWER BUD WORMWOOD VANILLYL BUTYL ETHER

🎯 Purpose 2 words ▾

pain relief

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 85304-0032-01 · Guangzhou 85305-0002-01 · Henan →
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.