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Camphor 0.04 MG/MG / menthol 0.1 MG/MG Topical Gel — RxCUI 1039731

RxNorm drug concept · Semantic clinical drug
RxCUI 1039731 Semantic clinical drug · SCD ● Current RxNorm concept 9 FDA products 10 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

RxCUI1039731
Official nameCamphor 0.04 MG/MG / menthol 0.1 MG/MG Topical Gel
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known ascamphor 4 % / menthol 10 % Topical Gel
FDA products mapped9
Package NDCs mapped10
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 0.04 MG/MG / menthol 0.1 MG/MG Topical G... 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 0.04 MG/MG / menthol 0.1 MG/MG Topical Gel RxCUI 1039731

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

  1. Ingredients 3

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

    • Camphor 1952
    • Menthol 6750
    • Camphor / menthol 466600
  2. Dose forms 4

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

    • Camphor / menthol Topical Gel 378021
    • Camphor / menthol Topical Product 1155407
    • Topical Gel 346286
    • Topical Product 1151122
  3. Clinical & branded drugs 2

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

    • Camphor 0.04 MG/MG 336103
    • Menthol 0.1 MG/MG 384557

Showing up to 8 concepts per family — 9 of 9 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 0.04 MG/MG SCDC · 336103
  • Menthol 0.1 MG/MG SCDC · 384557
  • Camphor / menthol Topical Gel SCDF · 378021
  • Camphor / menthol Topical Product SCDG · 1155407

📦 FDA Products & Package NDCs

9 products · 10 package NDCs
10 package NDCs map to RxCUI 1039731 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
59088-0083-00 1 KIT in 1 PACKAGE (59088-083-00) * 9 BLISTER PACK in 1 CA... Migranow PureTek Corporation 2016-04-18
59088-0259-07 85 g in 1 BOTTLE, WITH APPLICATOR (59088-259-07) Camphor 4% Plus Menthol 10% PureTek Corporation 2025-08-20
59088-0283-07 85 g in 1 BOTTLE, WITH APPLICATOR (59088-283-07) Camphotrex PureTek Corporation 2016-04-12
59088-0488-07 85 g in 1 BOTTLE, WITH APPLICATOR (59088-488-07) Camphotrol PureTek Corporation 2022-01-18
59088-0802-00 1 KIT in 1 KIT (59088-802-00) * 1 BOTTLE, DROPPER in 1 CAR... Diclogen PureTek Corporation 2024-07-26
70039-0283-07 1 g in 1 BOTTLE, WITH APPLICATOR (70039-283-07) Professional Therapy MuscleCare pain relieving gel Extra Strength Active and Innovative Inc. 2015-06-01
70039-0301-03 85 g in 1 BOTTLE, WITH APPLICATOR (70039-301-03) Professional Therapy MuscleCare Pro Roll-on ACTIVE AND INNOVATIVE, LLC 2024-04-30
70039-0302-16 453 g in 1 BOTTLE, PUMP (70039-302-16) Professional Therapy MuscleCare Pro Pain Relieving Cold Gel ACTIVE AND INNOVATIVE, LLC 2024-05-03
70039-0302-32 906 g in 1 BOTTLE, PUMP (70039-302-32) Professional Therapy MuscleCare Pro Pain Relieving Cold Gel ACTIVE AND INNOVATIVE, LLC 2024-05-03
81790-0001-00 88.7 mL in 1 BOTTLE, WITH APPLICATOR (81790-001-00) Relieve and Relax Pain Relieving MAC Innovations, LLC 2021-06-01
Observed labelers: PureTek Corporation (5) · ACTIVE AND INNOVATIVE, LLC (3) · Active and Innovative Inc. (1) · MAC Innovations, LLC (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.