Topcare Medicated Pain Relieving Patch 60ct Topcare Pain Relief Patch Extra Strength 60 mg/g; 31 mg/g; 100 mg/g Patch, 1 pouch
🆔 Identity & classification
Where does this data come from?
🏭 Manufacturer & labeler
Where does this data come from?
🩺 Clinical
This is an over-the-counter medicated patch designed to be applied to the skin for localized pain relief. It contains menthol, camphor, and methyl salicylate, which are topical analgesics and counterirritants commonly used to produce a cooling or warming sensation and to reduce minor muscle and joint aches. The patch delivers these ingredients directly to the affected area. This product is marketed under FDA's monograph rules for topical pain-relief products rather than as an individually approved application.
Patient education
Supplement & herbal interactions
Where does this data come from?
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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.
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Aluminum silicate is a mineral compound used as a thickener, absorbent, and anti-caking agent in medicines. It helps give liquid or powder formulations the right texture and prevents clumping.
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BHT is a synthetic antioxidant that prevents fats and oils in medicines from breaking down and becoming rancid. It helps keep the product stable and effective during storage.
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Glyceryl rosinate is a sticky substance made by combining rosin (a natural resin from pine trees) with glycerin. It's used in medicines as a binder to help hold solid ingredients together and improve texture and spreadability in certain formulations.
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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.
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A natural rubber material derived from the rubber tree. It's used as a coating or component in capsule shells and drug delivery devices to provide structure, flexibility, and controlled release of the medication.
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Paraffin is a waxy, petroleum-derived substance used as a coating, lubricant, and hardening agent in tablets and capsules. It helps protect the medicine from moisture and gives pills a smooth finish.
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A synthetic rubber-like polymer used as a binder and thickening agent in medicines. It helps hold tablet ingredients together and can improve the texture and consistency of formulations.
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Polyisobutylene is a synthetic rubber-like polymer used as a glidant and lubricant in tablet and capsule formulations. It reduces friction between particles and equipment during manufacturing and processing.
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A synthetic rubber-like plastic made from linked chains of styrene and isoprene. It's used in medicines as a binder to hold ingredients together and as a film-former to create protective coatings on tablets or capsules.
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Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.
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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.
11 inactive ingredients listed in the exact product block matched to this NDC.
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
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
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💲 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 system | Per each | Per 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. | |
Where does this data come from?
🔁 Therapeutic equivalents
Where does this data come from?
⏳ Availability & generic status
We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 36800-0750-60 You're viewing this | 1 POUCH in 1 BOX (36800-750-60) / 1 g in 1 POUCH | 2026-01-26 | Active |
🧭 About this NDC listing & data coverage
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. |
Questions about this listing
Is this NDC FDA-approved?
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Who lists this product with the FDA?
Do I need a prescription for this product?
Where does this data come from?
📄 FDA label — Drug Facts FDA SPL
🎯 Indications and Usage ▾
Directions adults and children 12 years of age and older: clean and dry affected area remove patch from film apply to affected area no more than 3 to 4 times daily do not wear patch for more than 4 hours children under 12 years of age: consult a doctor
⏱️ Dosage and Administration ▾
Questions or comments? Call 1-888-423-0139 Distributed By TOPCO ASSOCIATES LLC ITASCA, IL 60143 @TOPCO UNXA0525 Questions? 1-888-423-0139 [email protected] www.topcarebrand.com MADE IN CHINA
⚠️ Warnings ▾
Warnings For external use only.
📦 Storage and Handling ▾
Other information store at room temperature 20-25ºC (68-77º) avoid storing product in direct sunlight protect product from excessive moisture
🧪 Active Ingredient ▾
Active ingredients Purpose Camphor 3.1%............................................................Topical analgesic Menthol 6.0%..............................................................Topical analgesic Methyl salicylate 10.0%...............................................Topical analgesic
🧪 Inactive Ingredients ▾
Inactive ingredients aluminum silicate, butylated hydroxytoluene, glyceryl rosinate, lanolin, natural rubber, paraffin, polyisobutylene (85000 MW), polyisobutylene (800000 MW), styrene-isoprene-styrene block copolymer, titanium dioxide, zinc oxide
🎯 Purpose ▾
Uses temporary relief of minor aches and pains of muscles and joints associated with: arthritis simple backache sprains bruises strains