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Menthol 5 MG/ML / pramoxine hydrochloride 10 MG/ML Topical Lotion — RxCUI 1293905

RxNorm drug concept · Semantic clinical drug
RxCUI 1293905 Semantic clinical drug · SCD ● Current RxNorm concept 2 FDA products 2 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

RxCUI1293905
Official nameMenthol 5 MG/ML / pramoxine hydrochloride 10 MG/ML Topical Lotion
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asmenthol 0.5 % / pramoxine hydrochloride 1 % Topical Lotion; menthol 0.5 % / pramoxine HCl 1 % Topical Lotion
FDA products mapped2
Package NDCs mapped2
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
  • It gives short-term relief from pain and itching from minor problems like sunburn, minor burns, insect bites, and poison ivy rashes. Some products are made for specific uses, like...
  • That depends on the product. Many say not more than 3 to 4 times daily, and some allow up to 5 times daily. Check your label and follow it closely.
  • No. It is for external use only. If it gets in your eyes, rinse thoroughly with water.
  • Can I use it inside the vagina or near my eyes?
📖 Read our full Pramoxine guide →

🕸️ Concept Web — How Menthol 5 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 5 MG/ML / pramoxine hydrochloride 10 MG/ML Topical Lotion RxCUI 1293905

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 Lotion 377752
    • Menthol / pramoxine hydrochloride Topical Lotion 2647509
    • Menthol / pramoxine Topical Product 1159811
    • Menthol / pramoxine hydrochloride Topical Product 2662073
    • Topical Lotion 316983
    • Topical Product 1151122
  3. Clinical & branded drugs 2

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

    • Menthol 5 MG/ML 340082
    • 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 5 MG/ML SCDC · 340082
  • Pramoxine hydrochloride 10 MG/ML SCDC · 828361
  • Menthol / pramoxine Topical Lotion SCDF · 377752
  • Menthol / pramoxine hydrochloride Topical Lotion SCDFP · 2647509
  • Menthol / pramoxine Topical Product SCDG · 1159811
  • Menthol / pramoxine hydrochloride Topical Product SCDGP · 2662073

📦 FDA Products & Package NDCs

2 products · 2 package NDCs
2 package NDCs map to RxCUI 1293905 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
41167-0507-00 155 g in 1 BOTTLE (41167-0507-0) Gold Bond Intensive Relief Anti-Itch Chattem, Inc. 2016-04-26
84714-0507-00 155 g in 1 BOTTLE (84714-0507-0) Gold Bond Medicated Anti-Itch Gold Bond Co LLC 2016-04-26
Observed labelers: Chattem, Inc. (1) · Gold Bond Co 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.