Histamine dihydrochloride 0.3 MG/ML / menthol 30 MG/ML Topical Cream — RxCUI 2611792
RxNorm drug concept · Semantic clinical drug
RxCUI 2611792
Semantic clinical drug · SCD
● Current RxNorm concept 1 FDA product
1 package NDC
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
RxCUI2611792
Official nameHistamine dihydrochloride 0.3 MG/ML / menthol 30 MG/ML Topical Cream
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known ashistamine dihydrochloride 0.03 % / menthol 3 % Topical Cream
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 Menthol: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- Mostly for temporary relief of minor aches and pains in muscles and joints, like those from arthritis, backache, strains, sprains and bruises. Some products are for other things, s...
- It depends on the product. Many creams, gels and patches are limited to about 3 to 4 times a day, and patches also have a time limit, often 8 hours. Follow your product label and a...
- A brief burning feeling can happen when you first apply it and usually fades in several days. But if you get severe burning pain, swelling or blistering, stop using it and call you...
- No. Don't use menthol products with a heating pad, and avoid local heat or direct sunlight on the area. Rare cases of serious burns have been reported.
🕸️ Concept Web — How Histamine dihydrochloride 0.3 MG/ML / menthol 30... 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
Histamine dihydrochloride 0.3 MG/ML / menthol 30 MG/ML Topical Cream
RxCUI 2611792 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
-
Ingredients 4
The active substance itself — no strength, form, or brand attached yet.
-
Histamine
5333IN -
Menthol
6750IN -
Histamine / menthol
1007296MIN -
Histamine dihydrochloride
142136PIN
-
Histamine
-
Dose forms 6
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
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Histamine / menthol Topical Cream
707582SCDF -
Histamine dihydrochloride / menthol Topical Cream
2645420SCDFP -
Histamine / menthol Topical Product
1160918SCDG -
Histamine dihydrochloride / menthol Topical Product
2662150SCDGP -
Topical Cream
316982DF -
Topical Product
1151122DFG
-
Histamine / menthol Topical Cream
-
Clinical & branded drugs 2
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
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Histamine dihydrochloride 0.3 MG/ML
2167854SCDC -
Menthol 30 MG/ML
340105SCDC
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Histamine dihydrochloride 0.3 MG/ML
Showing up to 8 concepts per family — 12 of 12 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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Histamine dihydrochloride 0.3 MG/ML
SCDC · 2167854 -
Menthol 30 MG/ML
SCDC · 340105 -
Histamine / menthol Topical Cream
SCDF · 707582 -
Histamine dihydrochloride / menthol Topical Cream
SCDFP · 2645420 -
Histamine / menthol Topical Product
SCDG · 1160918 -
Histamine dihydrochloride / menthol Topical Product
SCDGP · 2662150
📦 FDA Products & Package NDCs
1 product · 1 package NDC
1 package NDC map to RxCUI 2611792 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 |
|---|---|---|---|---|
| 71067-0359-00 | 85 g in 1 BOTTLE, WITH APPLICATOR (71067-359-00) | DR. MIKES Ponos Pain Relief Cream Roll-On | Dr. Mike's Vitamins, LLC | 2022-08-29 |
Observed labelers:
Dr. Mike's Vitamins, 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.
Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.