Imiquimod 37.5 MG/ML Topical Cream — RxCUI 967017
RxNorm drug concept · Semantic clinical drug
RxCUI 967017
Semantic clinical drug · SCD
● Current RxNorm concept 6 FDA products
8 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
RxCUI967017
Official nameImiquimod 37.5 MG/ML Topical Cream
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asimiquimod 3.75 % Topical Cream
FDA products mapped6
Package NDCs mapped8
Reported Medicaid activity (SDUD)610 prescriptions · 8 state & territory Medicaid programs · latest period Q4 2025
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
📖 Skip the Codes — Read It in Plain English.
Our pharmacist-built guide to Imiquimod Topical: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- Imiquimod 5% cream treats actinic keratosis on the face or scalp, certain superficial basal cell carcinomas, and external genital or perianal warts. Which one you use it for decide...
- Wash the area with mild soap and let it dry. Put the cream on before bed and rub it in until it vanishes. Wash it off with mild soap and water after the recommended hours. Wash you...
- Yes, local skin reactions are very common. Expect redness, itching, burning, flaking and crusting. If the skin weeps, breaks open, or you feel flu-like, call your doctor. A rest pe...
- Is it normal for my skin to get red and sore?
🕸️ Concept Web — How Imiquimod 37.5 MG/ML Topical Cream 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
Imiquimod 37.5 MG/ML Topical Cream
RxCUI 967017 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
-
Ingredients 1
The active substance itself — no strength, form, or brand attached yet.
-
Imiquimod
59943IN
-
Imiquimod
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
-
Zyclara
967018BN
-
Zyclara
-
Dose forms 6
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
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Imiquimod Topical Cream
378638SCDF -
Imiquimod Topical Product
1160686SCDG -
Imiquimod Topical Cream [Zyclara]
967020SBDF -
Zyclara Topical Product
1186479SBDG -
Topical Cream
316982DF -
Topical Product
1151122DFG
-
Imiquimod Topical Cream
-
Clinical & branded drugs 3
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
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Imiquimod 37.5 MG/ML
967016SCDC -
Imiquimod 37.5 MG/ML Topical Cream [Zyclara]
967021SBD -
Imiquimod 37.5 MG/ML [Zyclara]
967019SBDC
-
Imiquimod 37.5 MG/ML
Showing up to 8 concepts per family — 11 of 11 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
-
Imiquimod 37.5 MG/ML
SCDC · 967016 -
Imiquimod Topical Cream
SCDF · 378638 -
Imiquimod Topical Product
SCDG · 1160686
Brand-Name Concepts
-
Imiquimod 37.5 MG/ML Topical Cream [Zyclara]
SBD · 967021 -
Imiquimod 37.5 MG/ML [Zyclara]
SBDC · 967019 -
Imiquimod Topical Cream [Zyclara]
SBDF · 967020 -
Zyclara Topical Product
SBDG · 1186479 -
Zyclara
BN · 967018
📦 FDA Products & Package NDCs
6 products · 8 package NDCs
8 package NDCs map to RxCUI 967017 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 |
|---|---|---|---|---|
| 00093-3133-31 | 1 BOTTLE, PUMP in 1 CARTON (0093-3133-31) / 7.5 g in 1 BOTT... | Imiquimod | Teva Pharmaceuticals USA, Inc. | 2020-07-30 |
| 51672-4174-06 | 28 PACKET in 1 CARTON (51672-4174-6) / .25 g in 1 PACKET (5... | Imiquimod | Sun Pharmaceutical Industries, Inc. | 2021-01-26 |
| 51672-4174-09 | 1 BOTTLE, PUMP in 1 CARTON (51672-4174-9) / 7.5 g in 1 BOTT... | Imiquimod | Sun Pharmaceutical Industries, Inc. | 2021-10-14 |
| 68682-0272-75 | 1 BOTTLE, PUMP in 1 CARTON (68682-272-75) / 7.5 g in 1 BOTT... | Imiquimod | Oceanside Pharmacueticals | 2018-06-27 |
| 99207-0270-01 | 4 PACKET in 1 CARTON (99207-270-01) / .25 g in 1 PACKET | Zyclara | Bausch Health US, LLC | 2011-11-28 |
| 99207-0271-01 | 1 BOTTLE, PUMP in 1 CARTON (99207-271-01) / 7.5 g in 1 BOTT... | Zyclara | Bausch Health US, LLC | 2012-01-01 |
| 99207-0271-75 | 1 BOTTLE, PUMP in 1 CARTON (99207-271-75) / 7.5 g in 1 BOTT... | Zyclara | Bausch Health US, LLC | 2012-01-01 |
| 99207-0276-01 | 1 BOTTLE, PUMP in 1 CARTON (99207-276-01) / 7.5 g in 1 BOTT... | Zyclara | Bausch Health US, LLC | 2012-02-29 |
Observed labelers:
Bausch Health US, LLC (4) ·
Sun Pharmaceutical Industries, Inc. (2) ·
Oceanside Pharmacueticals (1) ·
Teva Pharmaceuticals USA, Inc. (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.