Diphenhydramine hydrochloride 50 MG Oral Tablet [Somnapure] — RxCUI 1609070
RxNorm drug concept · Semantic branded drug
RxCUI 1609070
Semantic branded drug · SBD
● 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
RxCUI1609070
Official nameDiphenhydramine hydrochloride 50 MG Oral Tablet [Somnapure]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known asSomnapure 50 MG Oral Tablet; Somnapure Clinical Strength 50 MG Oral Tablet
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 Diphenhydramine Topical: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- It gives temporary relief of pain and itching on the skin. That includes minor burns, minor cuts or scrapes, insect bites, minor skin irritations, and rashes from poison ivy, oak o...
- Adults and children 2 and older can apply it to the affected area no more than 3 to 4 times a day. Don't use it more often than directed. For a child under 2, check with a doctor f...
- No. Don't use it on large areas of the body or on broken, blistered or oozing skin. Also avoid it on chicken pox or sunburn.
- Can I put it on a large area or on blistered skin?
🕸️ Concept Web — How Diphenhydramine hydrochloride 50 MG Oral Tablet... 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
Diphenhydramine hydrochloride 50 MG Oral Tablet [Somnapure]
RxCUI 1609070 Semantic branded drug · SBD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
-
Ingredients 2
The active substance itself — no strength, form, or brand attached yet.
-
Diphenhydramine
3498IN -
Diphenhydramine hydrochloride
1362PIN
-
Diphenhydramine
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
-
Somnapure
1609065BN
-
Somnapure
-
Dose forms 13
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
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Diphenhydramine Oral Tablet
371892SCDF -
Diphenhydramine hydrochloride Oral Tablet
2649122SCDFP -
Diphenhydramine Oral Product
1158449SCDG -
Diphenhydramine Pill
1158450SCDG -
Diphenhydramine hydrochloride Oral Product
2659104SCDGP -
Diphenhydramine hydrochloride Pill
2659100SCDGP -
Diphenhydramine Oral Tablet [Somnapure]
1609067SBDF -
Diphenhydramine hydrochloride Oral Tablet [Somnapure]
2655980SBDFP - +5 more in this family
-
Diphenhydramine Oral Tablet
-
Clinical & branded drugs 3
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
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Diphenhydramine hydrochloride 50 MG Oral Tablet
1085945SCD -
Diphenhydramine hydrochloride 50 MG
1020476SCDC -
Diphenhydramine hydrochloride 50 MG [Somnapure]
1609066SBDC
-
Diphenhydramine hydrochloride 50 MG Oral Tablet
Showing up to 8 concepts per family — 14 of 19 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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Diphenhydramine hydrochloride 50 MG Oral Tablet
SCD · 1085945 -
Diphenhydramine hydrochloride 50 MG
SCDC · 1020476 -
Diphenhydramine Oral Tablet
SCDF · 371892 -
Diphenhydramine hydrochloride Oral Tablet
SCDFP · 2649122 -
Diphenhydramine Oral Product
SCDG · 1158449 -
Diphenhydramine Pill
SCDG · 1158450 -
Diphenhydramine hydrochloride Oral Product
SCDGP · 2659104 -
Diphenhydramine hydrochloride Pill
SCDGP · 2659100
Brand-Name Concepts
-
Diphenhydramine hydrochloride 50 MG [Somnapure]
SBDC · 1609066 -
Diphenhydramine Oral Tablet [Somnapure]
SBDF · 1609067 -
Diphenhydramine hydrochloride Oral Tablet [Somnapure]
SBDFP · 2655980 -
Somnapure Oral Product
SBDG · 1609068 -
Somnapure Pill
SBDG · 1609069 -
Somnapure
BN · 1609065
📦 FDA Products & Package NDCs
1 product · 1 package NDC
1 package NDC map to RxCUI 1609070 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 |
|---|---|---|---|---|
| 69721-0005-30 | 1 BOTTLE in 1 CARTON (69721-005-30) / 30 TABLET, COATED in... | Somnapure Clinical Strength | Force Factor Brands LLC | 2018-03-20 |
Observed labelers:
Force Factor Brands 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.