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Lidocaine hydrochloride 0.04 MG/MG Topical Gel [Derma Numb] — RxCUI 1747492

RxNorm drug concept · Semantic branded drug
RxCUI 1747492 Semantic branded drug · SBD ● Current RxNorm concept 2 FDA products 3 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

RxCUI1747492
Official nameLidocaine hydrochloride 0.04 MG/MG Topical Gel [Derma Numb]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known asDerma Numb 4 % Topical Gel; Derma Numb 0.04 MG/MG Topical Gel
FDA products mapped2
Package NDCs mapped3
RxNorm release07/06/2026
Snapshot dataJul 14, 2026

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🕸️ Concept Web — How Lidocaine hydrochloride 0.04 MG/MG Topical Gel [... 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 Lidocaine hydrochloride 0.04 MG/MG Topical Gel [Derma Numb] RxCUI 1747492

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

  1. Ingredients 2

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

    • Lidocaine 6387
    • Lidocaine hydrochloride 142440
  2. Brand names 1

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

    • Derma Numb 1312261
  3. Dose forms 9

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

    • Lidocaine Topical Gel 377965
    • Lidocaine hydrochloride Topical Gel 2648601
    • Lidocaine Topical Product 1164666
    • Lidocaine hydrochloride Topical Product 2661923
    • Lidocaine Topical Gel [Derma Numb] 1747491
    • Lidocaine hydrochloride Topical Gel [Derma Numb] 2658475
    • Derma Numb Topical Product 1312264
    • Topical Gel 346286
    • +1 more in this family
  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 — 14 of 15 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

  • Lidocaine hydrochloride 0.04 MG/MG Topical Gel SCD · 1010077
  • Lidocaine hydrochloride 0.04 MG/MG SCDC · 1010076
  • Lidocaine Topical Gel SCDF · 377965
  • Lidocaine hydrochloride Topical Gel SCDFP · 2648601
  • Lidocaine Topical Product SCDG · 1164666
  • Lidocaine hydrochloride Topical Product SCDGP · 2661923

Brand-Name Concepts

  • Lidocaine hydrochloride 0.04 MG/MG [Derma Numb] SBDC · 1747490
  • Lidocaine Topical Gel [Derma Numb] SBDF · 1747491
  • Lidocaine hydrochloride Topical Gel [Derma Numb] SBDFP · 2658475
  • Derma Numb Topical Product SBDG · 1312264
  • Derma Numb BN · 1312261

📦 FDA Products & Package NDCs

2 products · 3 package NDCs
3 package NDCs map to RxCUI 1747492 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
70188-0005-01 28 g in 1 PACKAGE (70188-005-01) Derma Numb Pain Relief A.T.S. Laboratories, LLC 2015-07-01
70188-0005-04 113 g in 1 PACKAGE (70188-005-04) Derma Numb Pain Relief A.T.S. Laboratories, LLC 2015-07-01
70188-0006-01 57 g in 1 PACKAGE (70188-006-01) DermaNumb Analgesic A.T.S. Laboratories, LLC 2015-07-01
Observed labelers: A.T.S. Laboratories, LLC (3) — 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.