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Allantoin 0.02 MG/MG / benzethonium chloride 0.002 MG/MG / lidocaine hydrochloride 0.04 MG... — RxCUI 2566834

RxNorm drug concept · Semantic clinical drug
RxCUI 2566834 Semantic clinical drug · SCD ● Current RxNorm concept 1 FDA product 1 package NDC 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

RxCUI2566834
Official nameAllantoin 0.02 MG/MG / benzethonium chloride 0.002 MG/MG / lidocaine hydrochloride 0.04 MG/MG Oral Gel
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asallantoin 2 % / benzethonium chloride 0.2 % / lidocaine hydrochloride 4 % Oral Gel
FDA products mapped1
Package NDCs mapped1
RxNorm release07/06/2026
Snapshot dataJul 14, 2026

📖 Skip the Codes — Read It in Plain English.

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

📗 Our plain-language guide HelloPharmacist
  • It relieves nerve pain from post-herpetic neuralgia, the lingering pain that can follow shingles. It is used in adults. It numbs the pain signals in the skin under the patch.
  • Usually up to 12 hours in a 24-hour period, then 12 hours off. Put it on intact skin over the most painful spot. Do not use more patches than prescribed.
  • No. Heat can increase how much lidocaine gets absorbed. With Ztlido, you can apply a patch after brief heat, but never put a heating pad or electric blanket directly on it.
  • For Ztlido, light exercise and short water exposure, like a 10-minute shower, are okay. Gently pat it dry rather than rubbing. If the edges lift, press them down.
📖 Read our full Lidocaine Transdermal Patch guide →

🕸️ Concept Web — How Allantoin 0.02 MG/MG / benzethonium chloride 0.0... 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 Allantoin 0.02 MG/MG / benzethonium chloride 0.002 MG/MG / lidocaine hydrochloride 0.04 MG/MG Oral Gel RxCUI 2566834

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

  1. Ingredients 6

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

    • Allantoin 508
    • Benzethonium 1390
    • Lidocaine 6387
    • Allantoin / benzethonium / lidocaine 2566830
    • Benzethonium chloride 40036
    • Lidocaine hydrochloride 142440
  2. Dose forms 9

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

    • Allantoin / benzethonium / lidocaine Oral Gel 2566833
    • Allantoin / benzethonium chloride / lidocaine hydrochloride Oral Gel 2648226
    • Allantoin / benzethonium / lidocaine Oral Gel Product 2566832
    • Allantoin / benzethonium / lidocaine Oral Product 2566831
    • Allantoin / benzethonium chloride / lidocaine hydrochloride Oral Gel Product 2659225
    • Allantoin / benzethonium chloride / lidocaine hydrochloride Oral Product 2659543
    • Oral Gel 346169
    • Oral Gel Product 1294722
    • +1 more in this family
  3. Clinical & branded drugs 3

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

    • Allantoin 0.02 MG/MG 1540658
    • Benzethonium chloride 0.002 MG/MG 1011842
    • Lidocaine hydrochloride 0.04 MG/MG 1010076

Showing up to 8 concepts per family — 17 of 18 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

  • Allantoin 0.02 MG/MG SCDC · 1540658
  • Benzethonium chloride 0.002 MG/MG SCDC · 1011842
  • Lidocaine hydrochloride 0.04 MG/MG SCDC · 1010076
  • Allantoin / benzethonium / lidocaine Oral Gel SCDF · 2566833
  • Allantoin / benzethonium chloride / lidocaine hydrochloride Oral Gel SCDFP · 2648226
  • Allantoin / benzethonium / lidocaine Oral Gel Product SCDG · 2566832
  • Allantoin / benzethonium / lidocaine Oral Product SCDG · 2566831
  • Allantoin / benzethonium chloride / lidocaine hydrochloride Oral Gel Product SCDGP · 2659225
  • Allantoin / benzethonium chloride / lidocaine hydrochloride Oral Product SCDGP · 2659543

📦 FDA Products & Package NDCs

1 product · 1 package NDC
1 package NDC map to RxCUI 2566834 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
71687-4000-01 1 TUBE in 1 CARTON (71687-4000-1) / 4 g in 1 TUBE Herpecin Pain Relief Focus Consumer Healthcare, LLC 2021-06-11
Observed labelers: Focus Consumer Healthcare, 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.