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Menthol 10 MG/ML / pramoxine hydrochloride 10 MG/ML Topical Cream — RxCUI 1116155

RxNorm drug concept · Semantic clinical drug
RxCUI 1116155 Semantic clinical drug · SCD ● Current RxNorm concept 6 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

RxCUI1116155
Official nameMenthol 10 MG/ML / pramoxine hydrochloride 10 MG/ML Topical Cream
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asmenthol 1 % / pramoxine hydrochloride 1 % Topical Cream; menthol 1 % / pramoxine HCl 1 % Topical Cream
FDA products mapped6
Package NDCs mapped7
RxNorm release07/06/2026
Snapshot dataJul 14, 2026

📖 Skip the Codes — Read It in Plain English.

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

📗 Our plain-language guide HelloPharmacist
  • Pramoxine is a local anesthetic, which means it temporarily numbs the area where you apply it. It works right at the skin's surface to block the sensation of pain and itching. It d...
  • What exactly does pramoxine do — how does it stop the itching?
  • It depends on which product you have. Most creams, sprays, and solutions are used up to 3 to 4 times daily. Some products, like Proctofoam for the rectal area, can be used up to 5...
  • No. All pramoxine products are for external use only — that means the outside of the skin. Even products intended for the genital or rectal area, like the Terramed Intimate Wash or...
📖 Read our full Pramoxine guide →

🕸️ Concept Web — How Menthol 10 MG/ML / pramoxine hydrochloride 10 MG... 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 10 MG/ML / pramoxine hydrochloride 10 MG/ML Topical Cream RxCUI 1116155

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.

    • Menthol 6750
    • Pramoxine 34347
    • Menthol / pramoxine 691122
    • Pramoxine hydrochloride 57555
  2. Dose forms 6

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

    • Menthol / pramoxine Topical Cream 377753
    • Menthol / pramoxine hydrochloride Topical Cream 2646173
    • Menthol / pramoxine Topical Product 1159811
    • Menthol / pramoxine hydrochloride Topical Product 2662073
    • Topical Cream 316982
    • Topical Product 1151122
  3. Clinical & branded drugs 2

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

    • Menthol 10 MG/ML 340163
    • Pramoxine hydrochloride 10 MG/ML 828361

Showing up to 8 concepts per family — 12 of 12 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 10 MG/ML SCDC · 340163
  • Pramoxine hydrochloride 10 MG/ML SCDC · 828361
  • Menthol / pramoxine Topical Cream SCDF · 377753
  • Menthol / pramoxine hydrochloride Topical Cream SCDFP · 2646173
  • Menthol / pramoxine Topical Product SCDG · 1159811
  • Menthol / pramoxine hydrochloride Topical Product SCDGP · 2662073

📦 FDA Products & Package NDCs

6 products · 7 package NDCs
7 package NDCs map to RxCUI 1116155 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
53943-0265-01 1 TUBE in 1 CARTON (53943-265-01) / 28 g in 1 TUBE Freds Medicated anti itch Discount Drug Mart 2014-04-13
63868-0959-01 1 TUBE in 1 CARTON (63868-959-01) / 28 g in 1 TUBE QC Medicated anti itch Chain Drug Marketing Association 2020-12-07
63941-0265-01 1 TUBE in 1 CARTON (63941-265-01) / 28 g in 1 TUBE Best Choice Medicated anti itch value merchandisers 2014-04-13
65923-0104-14 1 TUBE in 1 CARTON (65923-104-14) / 14 g in 1 TUBE Family Care Maximum Strength Medicated Anti Itch United Exchange Corp. 2018-10-30
67234-0008-01 1 TUBE in 1 BOX (67234-008-01) / 42 g in 1 TUBE Anti Itch Maximum Relief Natureplex LLC 2008-01-02
69842-0265-01 1 TUBE in 1 CARTON (69842-265-01) / 28 g in 1 TUBE CVS Medicated anti itch CVS 2014-04-13
69842-0265-02 1 TUBE in 1 CARTON (69842-265-02) / 56 g in 1 TUBE CVS Medicated anti itch CVS 2014-04-13
Observed labelers: CVS (2) · Chain Drug Marketing Association (1) · Discount Drug Mart (1) · Natureplex LLC (1) · United Exchange Corp. (1) · value merchandisers (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.