Benzyl alcohol 2.7 MG/ML / zinc chloride 1.5 MG/ML Mucous Membrane Topical Solution — RxCUI 1865199
RxNorm drug concept · Semantic clinical drug
RxCUI 1865199
Semantic clinical drug · SCD
● Current RxNorm concept 1 FDA product
2 package NDCs
Snapshot Jul 14, 2026
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
RxCUI1865199
Official nameBenzyl alcohol 2.7 MG/ML / zinc chloride 1.5 MG/ML Mucous Membrane Topical Solution
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asbenzyl alcohol 0.27 % / zinc chloride 0.15 % Mucous Membrane Topical Solution
FDA products mapped1
Package NDCs mapped2
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
📖 Skip the Codes — Read It in Plain English.
Our pharmacist-built guide to Benzyl Alcohol Topical: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- Zilactin is designed to temporarily take the edge off pain from cold sores, fever blisters, canker sores, mouth sores, and gum irritations. It won't cure the sore or make it heal f...
- First, dry the sore area as best you can — this helps the gel stick and work properly. Then dab a small amount on the sore using a cotton swab or a clean finger. Let it sit and dry...
- It depends on age. Children 2 years and older can use Zilactin, but kids under 12 should always have an adult supervising. You should not use it at all on a child under 2 — check w...
- Don't use Zilactin for more than 7 days in a row unless your doctor or dentist specifically tells you to keep going. If the sore isn't improving by day 7, that's a sign something e...
🕸️ Concept Web — How Benzyl alcohol 2.7 MG/ML / zinc chloride 1.5 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
Benzyl alcohol 2.7 MG/ML / zinc chloride 1.5 MG/ML Mucous Membrane Topical Solution
RxCUI 1865199 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
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Ingredients 3
The active substance itself — no strength, form, or brand attached yet.
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Benzyl alcohol
1426IN -
Zinc chloride
39937IN -
Benzyl alcohol / zinc chloride
1865198MIN
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Benzyl alcohol
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Dose forms 4
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
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Benzyl alcohol / zinc chloride Mucous Membrane Topical Solution
1865197SCDF -
Benzyl alcohol / zinc chloride Mucosal Product
1865196SCDG -
Mucous Membrane Topical Solution
316956DF -
Mucosal Product
1151129DFG
-
Benzyl alcohol / zinc chloride Mucous Membrane Topical Solution
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Clinical & branded drugs 2
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
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Benzyl alcohol 2.7 MG/ML
1865194SCDC -
Zinc chloride 1.5 MG/ML
1865195SCDC
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Benzyl alcohol 2.7 MG/ML
Showing up to 8 concepts per family — 9 of 9 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
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Benzyl alcohol 2.7 MG/ML
SCDC · 1865194 -
Zinc chloride 1.5 MG/ML
SCDC · 1865195 -
Benzyl alcohol / zinc chloride Mucous Membrane Topical Solution
SCDF · 1865197 -
Benzyl alcohol / zinc chloride Mucosal Product
SCDG · 1865196
📦 FDA Products & Package NDCs
1 product · 2 package NDCs
2 package NDCs map to RxCUI 1865199 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 |
|---|---|---|---|---|
| 10237-0764-08 | 236.6 mL in 1 BOTTLE (10237-764-08) | Orajel Toothache Rinse | Church & Dwight Co., Inc. | 2016-12-01 |
| 10237-0764-16 | 473.2 mL in 1 BOTTLE (10237-764-16) | Orajel Toothache Rinse | Church & Dwight Co., Inc. | 2016-12-01 |
Observed labelers:
Church & Dwight Co., Inc. (2)
— 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.
Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.