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Benzocaine 0.2 MG/MG / menthol 0.001 MG/MG / zinc chloride 0.0015 MG/MG Oral Gel — RxCUI 2266762

RxNorm drug concept · Semantic clinical drug
RxCUI 2266762 Semantic clinical drug · SCD ● Current RxNorm concept 5 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

RxCUI2266762
Official nameBenzocaine 0.2 MG/MG / menthol 0.001 MG/MG / zinc chloride 0.0015 MG/MG Oral Gel
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asbenzocaine 20 % / menthol 0.1 % / zinc chloride 0.15 % Oral Gel
FDA products mapped5
Package NDCs mapped7
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 Benzocaine 0.2 MG/MG / menthol 0.001 MG/MG / zin... 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 Benzocaine 0.2 MG/MG / menthol 0.001 MG/MG / zinc chloride 0.0015 MG/MG Oral Gel RxCUI 2266762

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.

    • Benzocaine 1399
    • Menthol 6750
    • Zinc chloride 39937
    • Benzocaine / menthol / zinc chloride 1876613
  2. Dose forms 6

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

    • Benzocaine / menthol / zinc chloride Oral Gel 2362012
    • Benzocaine / menthol / zinc chloride Oral Gel Product 2362010
    • Benzocaine / menthol / zinc chloride Oral Product 2362011
    • Oral Gel 346169
    • Oral Gel Product 1294722
    • Oral Product 1151131
  3. Clinical & branded drugs 3

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

    • Benzocaine 0.2 MG/MG 340000
    • Menthol 0.001 MG/MG 440882
    • Zinc chloride 0.0015 MG/MG 2117333

Showing up to 8 concepts per family — 13 of 13 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

  • Benzocaine 0.2 MG/MG SCDC · 340000
  • Menthol 0.001 MG/MG SCDC · 440882
  • Zinc chloride 0.0015 MG/MG SCDC · 2117333
  • Benzocaine / menthol / zinc chloride Oral Gel SCDF · 2362012
  • Benzocaine / menthol / zinc chloride Oral Gel Product SCDG · 2362010
  • Benzocaine / menthol / zinc chloride Oral Product SCDG · 2362011

📦 FDA Products & Package NDCs

5 products · 7 package NDCs
7 package NDCs map to RxCUI 2266762 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
00363-1605-19 1 TUBE in 1 CARTON (0363-1605-19) / 11.9 g in 1 TUBE 3x Medicated Mouth Sore Gel Walgreens 2021-10-20
10237-0783-12 1 TUBE in 1 CARTON (10237-783-12) / 3.5 g in 1 TUBE Orajel 3X Medicated For All Mouth Sores Church & Dwight Co., Inc. 2019-11-01
10237-0783-18 1 TUBE in 1 CARTON (10237-783-18) / 5.1 g in 1 TUBE Orajel 3X Medicated For All Mouth Sores Church & Dwight Co., Inc. 2019-11-01
10237-0783-42 1 TUBE in 1 CARTON (10237-783-42) / 11.9 g in 1 TUBE Orajel 3X Medicated For All Mouth Sores Church & Dwight Co., Inc. 2019-11-01
11822-6170-09 1 TUBE in 1 CARTON (11822-6170-9) / 11.9 g in 1 TUBE 3X Medicated Mouth Sore Gel Rite Aid 2020-06-05
37808-0691-19 1 TUBE in 1 CARTON (37808-691-19) / 9.4 g in 1 TUBE 3x Medicated Mouth Sore Gel HEB 2020-06-02
69842-0660-09 1 TUBE in 1 CARTON (69842-660-09) / 11.9 g in 1 TUBE 3x Medicated Mouth Sore Gel CVS 2020-06-05
Observed labelers: Church & Dwight Co., Inc. (3) · CVS (1) · HEB (1) · Rite Aid (1) · Walgreens (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.

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Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.