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Camphor 0.012 MG/MG / menthol 0.057 MG/MG / methyl salicylate 0.063 MG/MG Medicated Patch — RxCUI 853260

RxNorm drug concept · Semantic clinical drug
RxCUI 853260 Semantic clinical drug · SCD ● Current RxNorm concept 7 FDA products 7 package NDCs Snapshot Jul 14, 2026

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Compiled from public NLM RxNorm and FDA (openFDA NDC directory) data sources. Editorial policy

What you’re looking at: the standardized identity of one medicine, as the U.S. drug-data system sees it. Below — every FDA-listed product, package code, price benchmark, and billing code that maps to it.

🗂️ Key Facts

RxCUI853260
Official nameCamphor 0.012 MG/MG / menthol 0.057 MG/MG / methyl salicylate 0.063 MG/MG Medicated Patch
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known ascamphor 1.2 % / menthol 5.7 % / methyl salicylate 6.3 % Medicated Patch
FDA products mapped7
Package NDCs mapped7
RxNorm release07/06/2026
Snapshot dataJul 14, 2026

📖 Skip the Codes — Read It in Plain English.

Our pharmacist-built guide to Menthol: what it is, how it’s used, side effects, and interactions.

📗 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 →

🕸️ Concept Web — How Camphor 0.012 MG/MG / menthol 0.057 MG/MG / meth... Connects

One RxCUI never lives alone. Follow the path from the raw ingredient down to the exact strength-and-form concepts FDA products carry — every stop is a real RxNorm concept with its own identifier. Hover or focus any chip for what it means.
This page's concept Camphor 0.012 MG/MG / menthol 0.057 MG/MG / methyl salicylate 0.063 MG/MG Medicated Patch RxCUI 853260

Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.

  1. Ingredients 4

    The active substance itself — no strength, form, or brand attached yet.

    • Camphor 1952
    • Menthol 6750
    • Methyl salicylate 29787
    • Camphor / menthol / methyl salicylate 691188
  2. Dose forms 4

    The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.

    • Camphor / menthol / methyl salicylate Medicated Patch 1792870
    • Camphor / menthol / methyl salicylate Topical Product 1155400
    • Medicated Patch 1792831
    • Topical Product 1151122
  3. Clinical & branded drugs 3

    Ingredient + strength + dose form. These are the concepts real FDA products actually carry.

    • Camphor 0.012 MG/MG 853257
    • Menthol 0.057 MG/MG 853258
    • Methyl salicylate 0.063 MG/MG 853259

Showing up to 8 concepts per family — 11 of 11 stored related concepts drawn.
These are official RxNorm vocabulary relationships — how concepts name and organize the same medicine. They do not establish therapeutic equivalence or substitutability: two concepts appearing in one web is never a statement that products can be swapped.

🔀 Generic ⇄ Brand Crosswalk

The same medicine has an unbranded (generic) identity and one or more brand-name identities — each with its own RxCUI. This is a naming relationship in RxNorm, not a statement that any two products are substitutable.

Generic (Clinical) Concepts

  • Camphor 0.012 MG/MG SCDC · 853257
  • Menthol 0.057 MG/MG SCDC · 853258
  • Methyl salicylate 0.063 MG/MG SCDC · 853259
  • Camphor / menthol / methyl salicylate Medicated Patch SCDF · 1792870
  • Camphor / menthol / methyl salicylate Topical Product SCDG · 1155400

📦 FDA Products & Package NDCs

7 products · 7 package NDCs
7 package NDCs map to RxCUI 853260 in the current snapshot — up to 50 per page. Each linked NDC opens its full package page.
Package NDC Package Brand / generic name Labeler Marketing start
00363-9903-40 40 POUCH in 1 BOX (0363-9903-40) / 9 g in 1 POUCH Pain Relieving Patches Walgreen Company 2019-11-15
29784-0600-01 1 KIT in 1 KIT (29784-600-01) * 4 PATCH in 1 KIT / .36 g i... Profoot Pain Relief Patches Rooftop Consumer Health, Inc. 2018-09-26
29784-0601-01 1 KIT in 1 KIT (29784-601-01) * 1 PATCH in 1 KIT / .36 g i... Profoot Pain Relief Patches Profoot, Inc. 2023-10-12
29784-0602-01 1 POUCH in 1 BOX (29784-602-01) / 4 PATCH in 1 POUCH / 1.03... Profoot Plantar Relief Strips Rooftop Consumer Health, Inc. 2023-10-18
36800-0670-40 40 PATCH in 1 CARTON (36800-670-40) / 1 g in 1 PATCH TopCare Health Pain Relief Topco Associates LLC 2022-03-08
65923-0148-02 1 PATCH in 1 POUCH (65923-148-02) / 1 g in 1 PATCH Coralite Muscle and Joint Pain Relief United Exchange Corporation 2018-10-23
65923-0564-20 20 PATCH in 1 PACKAGE (65923-564-20) / 1 g in 1 PATCH Coralite Pain Relief United Exchange Corp. 2018-04-12
Observed labelers: Rooftop Consumer Health, Inc. (2) · Profoot, Inc. (1) · Topco Associates LLC (1) · United Exchange Corp. (1) · United Exchange Corporation (1) · Walgreen Company (1) — this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.

🗃️ Sources & Limits

Atlas generation902fddb9-e9c1-4004-bf4c-dba4d51037c7
openFDA export observedJul 14, 2026
RxNorm release07/06/2026
Methodology2026-07-full-catalog-v1
  • A shared RxCUI does not prove interchangeability. Products mapped to the same concept are not thereby equivalent or substitutable — equivalence is a separate, product-level determination.
  • Listing here does not establish approval or coverage. Appearing in this snapshot is a data observation, not an FDA approval status or a payer coverage decision.
  • Missing data never means zero. A silent dataset (no price, no billing code, no utilization) means no observation — not that the real-world value is zero.
  • Counts describe the mapping footprint. Product, package, and labeler counts are the FDA-listed mapping footprint in this snapshot — not sales, inventory, availability, or market share.
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.

Machine-readable JSON

Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.