Home › NDC Lookup › RxCUI directory › RxCUI 2263170

Camphor 0.001 MG/MG / diphenhydramine hydrochloride 0.02 MG/MG / zinc acetate 0.01 MG/MG T... — RxCUI 2263170

Name: Camphor 0.001 MG/MG / diphenhydramine hydrochloride 0.02 MG/MG / zinc acetate 0.01 MG… (RxCUI 2263170)
Creator: Brian Staiger, PharmD

RxNorm drug concept · Semantic clinical drug

RxCUI 2263170 Semantic clinical drug · SCD ● Current RxNorm concept 2 FDA products 6 package NDCs Snapshot Jul 14, 2026

This page is curated, coded, and maintained by Dr. Brian Staiger, PharmD

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

RxCUI2263170

Official nameCamphor 0.001 MG/MG / diphenhydramine hydrochloride 0.02 MG/MG / zinc acetate 0.01 MG/MG Topical Gel

Concept typeSemantic clinical drug (SCD)

RxNorm statusCurrent RxNorm concept

Also known ascamphor 0.1 % / diphenhydramine HCl 2 % / zinc acetate 1 % Topical Gel; camphor 0.001 MG/MG / diphenhydramine HCl 0.02 MG/MG / zinc acetate 0.01 MG/MG Topical Gel

FDA products mapped2

Package NDCs mapped6

RxNorm release07/06/2026

Snapshot dataJul 14, 2026

📖 Skip the Codes — Read It in Plain English.

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

📗 Our plain-language guide HelloPharmacist

You can use it for temporary relief of pain and itching from everyday skin problems — things like insect bites, minor burns, minor cuts and scrapes, and general skin irritations. I...
What can I actually use this cream or spray for?
You can apply it up to 3 to 4 times a day, but no more than that. More frequent use isn't going to help more — and the label is clear that you shouldn't exceed that limit. For kids...
This is really important — do not use this topical product at the same time as any other product that contains diphenhydramine, even a pill or capsule. That includes allergy medici...

📖 Read our full Diphenhydramine Topical guide →

🕸️ Concept Web — How Camphor 0.001 MG/MG / diphenhydramine hydrochlor... 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 Camphor 0.001 MG/MG / diphenhydramine hydrochloride 0.02 MG/MG / zinc acetate 0.01 MG/MG Topical Gel RxCUI 2263170 Semantic clinical drug · SCD

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

Ingredients 5

The active substance itself — no strength, form, or brand attached yet.
- Camphor 1952 IN
- Diphenhydramine 3498 IN
- Zinc acetate 58295 IN
- Camphor / diphenhydramine / zinc acetate 2263169 MIN
- Diphenhydramine hydrochloride 1362 PIN
Dose forms 6

The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
- Camphor / diphenhydramine / zinc acetate Topical Gel 2263168 SCDF
- Camphor / diphenhydramine hydrochloride / zinc acetate Topical Gel 2648902 SCDFP
- Camphor / diphenhydramine / zinc acetate Topical Product 2263167 SCDG
- Camphor / diphenhydramine hydrochloride / zinc acetate Topical Product 2659113 SCDGP
- Topical Gel 346286 DF
- Topical Product 1151122 DFG
Clinical & branded drugs 3

Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
- Camphor 0.001 MG/MG 1440015 SCDC
- Diphenhydramine hydrochloride 0.02 MG/MG 1049088 SCDC
- Zinc acetate 0.01 MG/MG 334322 SCDC

Showing up to 8 concepts per family — 14 of 14 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

Camphor 0.001 MG/MG SCDC · 1440015
Diphenhydramine hydrochloride 0.02 MG/MG SCDC · 1049088
Zinc acetate 0.01 MG/MG SCDC · 334322
Camphor / diphenhydramine / zinc acetate Topical Gel SCDF · 2263168
Camphor / diphenhydramine hydrochloride / zinc acetate Topical Gel SCDFP · 2648902
Camphor / diphenhydramine / zinc acetate Topical Product SCDG · 2263167
Camphor / diphenhydramine hydrochloride / zinc acetate Topical Product SCDGP · 2659113

📦 FDA Products & Package NDCs

2 products · 6 package NDCs

6 package NDCs map to RxCUI 2263170 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
65753-0400-02	59 mL in 1 BOTTLE (65753-400-02)	CoreTex Anti-Itch Gel	CoreTex Products Inc	2019-11-26
65753-0400-04	177 mL in 1 BOTTLE (65753-400-04)	CoreTex Anti-Itch Gel	CoreTex Products Inc	2019-11-26
65753-0400-13	25 POUCH in 1 CONTAINER (65753-400-13) / 1 mL in 1 POUCH	CoreTex Anti-Itch Gel	CoreTex Products Inc	2019-11-26
65753-0400-14	300 POUCH in 1 CONTAINER (65753-400-14) / 1 mL in 1 POUCH	CoreTex Anti-Itch Gel	CoreTex Products Inc	2019-11-26
65753-0514-35	1 KIT in 1 KIT (65753-514-35) * 4.44 mL in 1 APPLICATOR (6...	CoreTex Professional Outdoor Skin Protection Wallet	CoreTex Products Inc	2023-02-24
65753-0514-36	1 KIT in 1 KIT (65753-514-36) * 4.44 mL in 1 APPLICATOR (6...	CoreTex Professional Outdoor Skin Protection Wallet	CoreTex Products Inc	2023-02-24

Observed labelers: CoreTex Products Inc (6) — 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.