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Menthol 12.5 MG/ML Topical Cream — RxCUI 416982

RxNorm drug concept · Semantic clinical drug
RxCUI 416982 Semantic clinical drug · SCD ● Current RxNorm concept 10 FDA products 16 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

RxCUI416982
Official nameMenthol 12.5 MG/ML Topical Cream
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asmenthol 1.25 % Topical Cream
FDA products mapped10
Package NDCs mapped16
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 Menthol 12.5 MG/ML Topical Cream 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 Menthol 12.5 MG/ML Topical Cream RxCUI 416982

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

  1. Ingredients 1

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

    • Menthol 6750
  2. Brand names 1

    The same medicine's trade names. A brand name alone says nothing about strength or form.

    • Celadrin 2380349
  3. Dose forms 6

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

    • Menthol Topical Cream 377751
    • Menthol Topical Product 1160376
    • Menthol Topical Cream [Celadrin] 2380351
    • Celadrin Topical Product 2380352
    • Topical Cream 316982
    • Topical Product 1151122
  4. Clinical & branded drugs 3

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

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

  • Menthol 12.5 MG/ML SCDC · 340115
  • Menthol Topical Cream SCDF · 377751
  • Menthol Topical Product SCDG · 1160376

Brand-Name Concepts

  • Menthol 12.5 MG/ML Topical Cream [Celadrin] SBD · 1046429
  • Menthol 12.5 MG/ML [Celadrin] SBDC · 2380354
  • Menthol Topical Cream [Celadrin] SBDF · 2380351
  • Celadrin Topical Product SBDG · 2380352
  • Celadrin BN · 2380349

📦 FDA Products & Package NDCs

10 products · 16 package NDCs
16 package NDCs map to RxCUI 416982 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
54230-0356-01 170 g in 1 JAR (54230-356-01) Celadrin Joint and Muscle Pain Relieving Factors Group of Nutritional Products 2012-10-01
70015-0665-01 1 TUBE in 1 CARTON (70015-665-01) / 28 g in 1 TUBE Instaflex Pain Relief Cream Healthy Directions, LLC 2020-06-10
70015-0665-02 1 TUBE in 1 CARTON (70015-665-02) / 57 g in 1 TUBE Instaflex Pain Relief Cream Healthy Directions, LLC 2019-01-01
70015-0665-04 1 TUBE in 1 CARTON (70015-665-04) / 113 g in 1 TUBE Instaflex Pain Relief Cream Healthy Directions, LLC 2019-01-01
70554-0229-00 1 TUBE in 1 BOX (70554-229-00) / 50 mL in 1 TUBE FEELGOOD LAB Natural Pain Cream The Feel Good Lab, LLC 2021-05-26
70554-0339-00 5 mL in 1 PACKET (70554-339-00) FEEL GOOD LAB Natural Pain Cream THE FEEL GOOD LAB, LLC 2022-07-15
72609-0045-04 1 JAR in 1 BOX (72609-045-04) / 114 g in 1 JAR Joint Ease Smith Amish, LLC 2024-08-28
72609-0702-02 59 g in 1 BOX (72609-702-02) ARTHRITIS Smith Amish, LLC 2024-08-28
72609-0702-04 123 g in 1 JAR (72609-702-04) ARTHRITIS Smith Amish, LLC 2025-08-01
72609-0703-02 1 TUBE in 1 BOX (72609-703-02) / 59 g in 1 TUBE FOOT Smith Amish, LLC 2024-08-28
72609-0703-04 123 g in 1 JAR (72609-703-04) FOOT Smith Amish, LLC 2025-08-01
72779-0100-02 1 TUBE in 1 CARTON (72779-100-02) / 57 g in 1 TUBE Instaflex Pain Relief Cream Adaptive Health, LLC 2019-01-01
72779-0100-04 1 TUBE in 1 CARTON (72779-100-04) / 113 g in 1 TUBE Instaflex Pain Relief Cream Adaptive Health, LLC 2019-01-01
72839-0371-01 5 mL in 1 BOTTLE (72839-371-01) Flexigen Derma Care Research Labs, LLC 2022-07-11
72839-0371-03 95 mL in 1 BOTTLE (72839-371-03) Flexigen Derma Care Research Labs, LLC 2022-07-11
84483-0001-01 1 TUBE in 1 BOX (84483-0001-1) / 50 g in 1 TUBE Teevodar Pain Relieving Sod-e Biotech Ltd 2024-09-01
Observed labelers: Smith Amish, LLC (5) · Healthy Directions, LLC (3) · Adaptive Health, LLC (2) · Derma Care Research Labs, LLC (2) · THE FEEL GOOD LAB, LLC (2) · Factors Group of Nutritional Products (1) · +1 more — 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.