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(from DailyMed)

Up and Up Cold and Hot Medicated Menthol 50 mg Patch

by TARGET CORP · 1 PATCH in 1 CARTON (11673-887-05) / 5 PATCH in 1 PATCH
NDC 11673-0887-05
🏷️ FDA NDC (as labeled) 11673-887-05 billing pads the product segment with a zero
OTC Discontinued Non-controlled ⚠ Discontinued by firm
🗂️ Data synced Jul 16, 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

⚠️
Other active recalls for Menthol (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Mar 20, 2026 — This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality. (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.) · FDA recall D-0458-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗
⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Jul 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

🆔 Identity & classification

FDA NDC (as labeled) 11673-887-05
Product NDC 11673-887
11-digit billing NDC 11673088705
RxCUI 420222
UNII L7T10EIP3A
UPC 0780707006788
Application # M017
SPL Set ID c5ecad63-0d42-33cd-e053-2995a90acef7
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Jul 2026)
Marketing start 2021-06-01
Marketing end 2026-07-17
Route TOPICAL
Dosage form PATCH
Substance MENTHOL
Why two NDCs? The FDA registers this code as 11673-887-05 — 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 → 11673-0887-05. 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

LabelerTARGET CORP
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code11673
First marketedJun 2021
Product typeHuman Otc Drug
Portfolio9 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

📗 Our plain-language guide HelloPharmacist
  • Menthol is found in a lot of over-the-counter topical products — creams, gels, patches, sprays, and powders. Depending on the product, it's used to temporarily ease minor muscle an...
  • Start with clean, dry skin — free of lotions or creams — before applying the patch. Peel the backing off and press the sticky side firmly to the sore area. Most menthol patches sho...
  • Yes, a mild burning or tingling feeling right after applying a menthol product is common and usually settles down within a few days of regular use. What's not normal is severe burn...
  • Is that burning sensation after I apply it normal?
📖 Read our full Menthol guide →

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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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 eachPer 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Extra Strength Cold-Hot Medicated Patches 5 g 70000-0367-01 Cardinal 5 patches $0.772 — FDA listed —
Rugby Menthol Hot Cold Patch 5 g/100g 00536-1332-15 RUGBY 5 patches $1.023 — Availability likely —
Good Neighbor Pharmacy Cold Therapy Pain Relief Patch 5 g/100g 46122-0751-45 Amerisource 5 patches $1.023 — Availability likely —
Walgreens Cool N Heat Back Patch 50 mg/g 00363-6657-05 Walgreen 5 patches — — FDA listed —
Walgreens Cold Therapy Pain Relieving Patch 50 mg/g 00363-6669-05 Walgreen 5 patches — — FDA listed —
Walgreens Cool N Heat Patch XL 50 mg/g 00363-6672-03 Walgreen 3 patches — — FDA listed —
Hot and Cold Medicated Patch 5 g/100g 00363-9520-05 Walgreen 5 pouches — — FDA listed —
Extra Large Cool and Heat Patch 5 g/100g 00363-9905-03 Walgreen 3 pouches — — FDA listed —
Walgreens Cold Therapy Pain Relief Patch 5 g/100g 00363-9950-05 Walgreens 5 patches — — FDA listed —
Cold and Hot Medicated 500 mg 10742-1117-01 The 5 patches — — FDA listed —
Cold and Hot Medicated 240 mg 10742-1118-01 The 5 patches — — FDA listed —
WellPatch Cooling Pain Relief 50 mg 10742-8125-01 The 1 patch — — Discontinued —
Up and Up Cold and Hot Medicated 50 mgthis 11673-0887-05 TARGET 1 patch — — Discontinued —
Extra Strength Cold and Hot Menthol Patch 5 g/100g 11822-6513-01 Rite 5 patches — — FDA listed —
Rite Aid Hot and Cold Back Patch 5 g/100g 11822-9991-03 Rite 3 patches — — FDA listed —
Signature Care Cold and Hot Medicated 50 mg 21130-0980-01 Safeway 5 patches — — FDA listed —
Signature Care Medicated Cold and Hot Patch 5 g/100g 21130-0987-05 Safeway 5 patches — — FDA listed —
Kroger Hot and Cold Medicated Patch 5 g/100g 30142-0979-05 Kroger 5 pouches — — FDA listed —
Topcare Cold and Hot Medicated 50 mg 36800-0860-05 Topco 5 patches — — FDA listed —
Icy Hot Back and Large Areas 5 g/100g 41167-0073-08 Chattem, 10 patches — — FDA listed —
Icy Hot Back and Large Areas 5 g/100g 41167-0083-02 Chattem, 1 patch — — FDA listed —
Icy Hot Arm Neck Leg and Small Areas 5 g/100g 41167-0084-01 Chattem, 5 patches — — FDA listed —
Icy Hot Back and Large Areas 5 g/100g 41167-0843-01 Chattem, 5 patches — — FDA listed —
Icy Hot XL Back and Large Areas 5 g/100g 41167-0847-01 Chattem, 3 patches — — FDA listed —
ICY Hot Value Pack 41167-0854-00 Chattem, 5 patches — — FDA listed —
Meijer Small Cold-Hot Medicated Patches 5 g 41250-0522-05 Meijer 5 patches — — FDA listed —
Meijer Large Cold-Hot Medicated Patches 5 g 41250-0834-05 Meijer 5 patches — — FDA listed —
Equate Menthol Pain Relieving 50 mg 49035-0870-01 Wal-Mart 1 patch — — FDA listed —
Equate Cool and Heat Extra Strength 50 mg 49035-0888-30 Wal-Mart 5 patches — — FDA listed —
Good Sense Hot and Cold Medicated Patch 5 g/100g 50804-0124-13 GOOD 5 pouches — — FDA listed —
Goodsense Extra Strength Cold and Hot Medicated 50 mg 50804-0126-05 Geiss, 5 patches — — FDA listed —
CVS Cooling Patch .5 g/10g 51316-0796-02 CVS 2 patches — — FDA listed —
CVS Health Cooling Patch 5 g/100g 51316-0976-10 CVS 10 patches — — FDA listed —
Cold And Hot Medicated Large .05 g/g 52000-0421-41 Universal 1 patch — — FDA listed —
Cold And Hot Medicated .05 g/g 52000-0422-41 Universal 2 patches — — FDA listed —
Medline 5 mg/100mg 53329-0972-05 Medline 5 patches — — FDA listed —
Menthol Pain Relief Gel Patch 50 mg 55629-0025-15 ONE2ZEE 15 patches — — FDA listed —
Dollar General Cold-Hot Medicated Patches 5 g/100g 55910-0903-01 DOLGENCORP, 1 pouch — — FDA listed —
Dollar General Cold Therapy Pain Relief 5 g/100g 55910-0949-01 Dolgencorp, 1 g — — FDA listed —
Dollar General Cold-Hot Medicated Patches 5 g 55910-0972-06 DOLGENCORP, 6 patches — — FDA listed —
Biofreeze Overnight Relief .3 g/6g 59316-0005-03 Reckitt 1 patch — — FDA listed —
Biofreeze Day and Overnight 59316-0832-94 Reckitt 1 patch — — FDA listed —
Biofreeze Menthol 59316-0887-04 Reckitt 1 patch — — FDA listed —
Biofreeze Menthol .05 g/g 59316-0992-07 Reckitt 1 patch — — FDA listed —
Icy Hot Medicated 205.5 mg 62168-0084-03 Lead 1350 patches — — Discontinued —
Icy Hot Medicated, XL 750 mg 62168-0847-04 Lead 400 patches — — FDA listed —
Icy Hot Medicated, Back 428.5 mg 62168-0853-01 Lead 500 patches — — FDA listed —
Winco Cold and Hot Medicated Patch Large 50 mg 67091-0914-05 WINCO 5 patches — — FDA listed —
Hot/Cold Medicated Patch 285 mg/5700mg 67777-0201-10 Dynarex 900 patches — — FDA listed —
Absorbine Jr 5000 mg/h 69693-0412-01 Clarion 1 patch — — FDA listed —
Icequake Coldn Hot medicated patch 50 mg/g 69822-0014-04 Southern 4 patches — — FDA listed —
CVS Cold and Hot 50 mg 69842-0243-05 CVS 5 patches — — FDA listed —
CVS Cold and Hot 50 mg 69842-0245-05 CVS 5 patches — — FDA listed —
Bengay Ultra Strength Large Size 50 mg 69968-0487-01 Kenvue 1 patch — — Discontinued —
HealthWise Medicated Cold Hot 5% Patch 5 g 71101-0031-06 Veridian 6 patches — — FDA listed —
Cold Hot Medicated Patch 5% Menthol 5 g 71101-0060-05 Veridian 5 patches — — FDA listed —
Cold Hot Medicated Patch 5% Menthol 5 g 71101-0061-05 Veridian 5 patches — — FDA listed —
HealthWise Medicated Cold Hot 5% 5 g 71101-0084-15 Veridian 15 patches — — FDA listed —
HealthWise Overnight Menthol Patch 5 g 71101-0085-12 Veridian 12 patches — — FDA listed —
TheraCare Pain Relief 5 g/100g 71101-0126-01 Veridian 4 patches — — FDA listed —
Thera Care Pain Relief Menthol Patchs 5 g/100g 71101-0913-05 Veridian 5 pouches — — FDA listed —
Theracare Cold Therapy Pain Relief 5 g 71101-0949-01 Veridian 5 patches — — FDA listed —
HealthWise Cold Therapy Pain Relief Patch 5 g/100g 71101-0950-15 Veridian 15 patches — — FDA listed —
Hot and Cold Medicated Patch 5 g/100g 71101-0952-15 Veridian 15 pouches — — FDA listed —
Thera Care Hot and Cold Medicated Patch 5 g/100g 71101-0953-05 Veridian 5 pouches — — FDA listed —
Thera Care Cold Hot Medicated Patch 5 g/100g 71101-0954-05 Veridian 5 pouches — — FDA listed —
Dr Sabharwals 240 mg 71318-0116-15 Dr. 15 patches — — FDA listed —
Menthol 5% 440 mg 71391-0123-18 Unexo 18 patches — — Discontinued —
Menthol 5% Hydrogel 600 mg 71391-0127-05 Unexo 5 patches — — Discontinued —
Cold Hot Medicated Patch 5% Menthol 5 g 71811-0005-05 InterMed 5 patches — — FDA listed —
Cold Hot Medicated Patch 5% Menthol 5 g 71811-0006-05 InterMed 5 patches — — FDA listed —
Hot and Cold Medicated Patch 5 g/100g 72036-0952-05 Harris 5 pouches — — FDA listed —
Amazon Basics Cold and Hot Medicated Patch 5 g/100g 72288-0966-15 Amazon.com 15 patches — — FDA listed —
Cycle 5 g/100g 72587-0001-02 La 1 patch — — FDA listed —
Relief 5 g/100g 72587-0003-01 La 4 patches — — FDA listed —
Hempvana Cold As Ice Pain Relief Gel-Patch 5 g/100g 73287-0005-01 Telebrands 7 patches — — FDA listed —
MENTHOL PAIN RELIEF Gel-Patch .05 g/g 73557-0131-15 Shanghai 15 patches — — Discontinued —
OVERNIGHT RELIEF Gel-Patch .05 g/g 73557-0133-05 Shanghai 5 patches — — FDA listed —
Pain Relief .05 g/g 73557-0192-05 Shanghai 5 patches — — FDA listed —
BonicaEaseX 24 Hour Menthol Pain Relieving 50 mg/g 75568-0045-00 Planet 15 patches — — FDA listed —
Topcare Pain Relief Patch 5 g/100g 76162-0999-05 76162 5 patches — — FDA listed —
Meijer Cold Therapy Pain Relieving 5 g/100g 79481-9966-05 Meijer 1 g — — FDA listed —
Menthol 5% 500 mg/10g 80425-0543-01 Advanced 30 patches — — FDA listed —
Cold Hot Medicated Patch 5% Menthol 5 g 83324-0256-05 Quality 5 patches — — FDA listed —
Hot Cold Medicated Patches 5 g/1001 83559-0003-01 Henan 2 patches — — FDA listed —
COLD AND HOT MEDICATED Patch 5 g/1001 83559-0014-01 Henan 48 patches — — FDA listed —
COLD AND HOT MEDICATED Patch 5 g/1001 83559-0015-01 Henan 24 patches — — FDA listed —
Rapid Relief 5 g/100g 83569-0012-05 RAPID 1 pouch — — FDA listed —
Menthol Pain Relief Gel-Patch .05 g/g 83602-0132-15 Guangzhou 15 patches — — FDA listed —
COLD HOT CHINESE RED TIGER PAIN RELIEF GeI-Patch .05 g/g 84165-0004-01 Guangzhou 12 g — — FDA listed —
AVCOO Menthol Pain Relief Patch 500 mg 84992-0004-01 ADP 1 patch — — FDA listed —
Menthol 5% 500 mg/10g 85096-0301-30 Marcella 30 patches — — FDA listed —
5% Menthol Pain Relief Patch 5 g/100g 85323-0004-00 Xuzhou 5 patches — — FDA listed —
5% Menthol Pain Relief Patch 5 g/100g 85323-0006-01 Xuzhou 48 patches — — FDA listed —
5% Menthol Pain Relief Patch 5 g/100g 85323-0007-01 Xuzhou 24 patches — — 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

🏛️
2021
On the market since
Jun 2021
📍
2026
Currently FDA-listed
5 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.

🔬 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 Menthol — the ingredient across all brands.

Top reported reactions

Pain3,550
Fatigue3,325
Nausea3,271
Headache3,025
Dyspnoea2,478
Diarrhoea2,214
Pneumonia2,153

Age at onset

Neonate144
Infant64
Child375
Adolescent265
Adult5,396
Elderly3,493

Reporter sex

54,517 reports
Male · 36%
Female · 63%
Unknown · 0%

Serious outcomes

Hospitalization18,810
Death5,295
Disabling1,342
Reports over time (by year) — tap or hover for the count & year
2022 2023 2024 2026 4,676 2,446
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
11673-0887-05 You're viewing this 1 PATCH in 1 CARTON (11673-887-05) / 5 PATCH in 1 PATCH 2021-11-11 Discontinued by firm

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product No longer marketed (per FDA listing data)
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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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 11673-887-05, 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: 11673-0887-05, written without dashes as 11673088705. 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 11673-0887-05, the first segment (11673) is the labeler code FDA assigned to TARGET CORP; the middle segment (0887) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (05) identifies this exact package size and type. Together they name one specific package of one specific product.
Who lists this product with the FDA?
TARGET CORP 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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 55 words ▾

Directions open pouch and remove patch carefully peel off protective backing and apply sticky side to affected area adults and children 12 years of age and older: do not wear patch for more than 8 hours apply to affected area no more than 3 times daily children under 12 years of age: consult a doctor

⏱️ Dosage and Administration 7 words ▾

Distributed by: Target Corporation Made in China

⚠️ Warnings 5 words ▾

Warnings For external use only

📦 Storage and Handling 8 words ▾

Other information store at room temperature 20-25°C (68-77°F)

🧪 Active Ingredient 6 words ▾

Active ingredient Purpose Menthol 5%...........................................................Topical analgesic

🧪 Inactive Ingredients 21 words ▾

Inactive ingredients alcohol, aluminum glycinate, glycerin, kaolin, methylparaben, polysorbate 80, propylparaben, purified water, sodium polyacrylate, sorbitan monooleate, tartaric acid, titanium dioxide

🎯 Purpose 19 words ▾

Uses temporarily relieves minor aches and pains of muscles and joints associated with: simple backache arthritis strains bruises sprains

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 11673-0880-44 · TARGET 11673-0890-56 · Target →
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.