Acetaminophen 500 MG / dextromethorphan hydrobromide 20 MG Powder for Oral Solution — RxCUI 2670598
RxNorm drug concept · Semantic clinical drug
RxCUI 2670598
Semantic clinical drug · SCD
● Current RxNorm concept 9 FDA products
13 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
RxCUI2670598
Official nameAcetaminophen 500 MG / dextromethorphan hydrobromide 20 MG Powder for Oral Solution
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asAPAP 500 MG / dextromethorphan hydrobromide 20 MG Powder for Oral Solution
FDA products mapped9
Package NDCs mapped13
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
📖 Skip the Codes — Read It in Plain English.
Our pharmacist-built guide to Acetaminophen Injection: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- Great question. The IV form is used when you can't take medication by mouth — for example, after surgery, if you're nauseated, or if you need faster, more reliable absorption. It d...
- Why am I getting acetaminophen through an IV instead of just taking a pill?
- Yes, Acetaminophen Injection is approved for children — for pain relief in kids 2 years and older, and for fever reduction in patients of all ages, including premature newborns bor...
- The most important things to watch for are signs of a serious allergic reaction — swelling of your face, mouth, or throat, trouble breathing, or hives — and any new skin rash. Eith...
🕸️ Concept Web — How Acetaminophen 500 MG / dextromethorphan hydrobro... 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
Acetaminophen 500 MG / dextromethorphan hydrobromide 20 MG Powder for Oral Solution
RxCUI 2670598 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.
-
Acetaminophen
161IN -
Dextromethorphan
3289IN -
Acetaminophen / dextromethorphan
214180MIN -
Dextromethorphan hydrobromide
102490PIN
-
Acetaminophen
-
Dose forms 9
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
-
Acetaminophen / dextromethorphan Powder for Oral Solution
2636655SCDF -
Acetaminophen / dextromethorphan hydrobromide Powder for Oral Solution
2648707SCDFP -
Acetaminophen / dextromethorphan Oral Powder Product
2603746SCDG -
Acetaminophen / dextromethorphan Oral Product
1151184SCDG -
Acetaminophen / dextromethorphan hydrobromide Oral Powder Product
2663082SCDGP -
Acetaminophen / dextromethorphan hydrobromide Oral Product
2662804SCDGP -
Powder for Oral Solution
1540455DF -
Oral Powder Product
1294711DFG - +1 more in this family
-
Acetaminophen / dextromethorphan Powder for Oral Solution
-
Clinical & branded drugs 2
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
-
Acetaminophen 500 MG
315266SCDC -
Dextromethorphan hydrobromide 20 MG
1037200SCDC
-
Acetaminophen 500 MG
Showing up to 8 concepts per family — 14 of 15 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
-
Acetaminophen 500 MG
SCDC · 315266 -
Dextromethorphan hydrobromide 20 MG
SCDC · 1037200 -
Acetaminophen / dextromethorphan Powder for Oral Solution
SCDF · 2636655 -
Acetaminophen / dextromethorphan hydrobromide Powder for Oral Solution
SCDFP · 2648707 -
Acetaminophen / dextromethorphan Oral Powder Product
SCDG · 2603746 -
Acetaminophen / dextromethorphan Oral Product
SCDG · 1151184 -
Acetaminophen / dextromethorphan hydrobromide Oral Powder Product
SCDGP · 2663082 -
Acetaminophen / dextromethorphan hydrobromide Oral Product
SCDGP · 2662804
📦 FDA Products & Package NDCs
9 products · 13 package NDCs
13 package NDCs map to RxCUI 2670598 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 |
|---|---|---|---|---|
| 00067-0100-06 | 6 PACKET in 1 CARTON (0067-0100-06) / 1 POWDER, FOR SOLUTIO... | Theraflu Severe Cold Relief Daytime | Haleon US Holdings LLC | 2023-12-01 |
| 00067-0100-99 | 1000 PACKET in 1 CONTAINER (0067-0100-99) / 1 POWDER, FOR S... | Theraflu Severe Cold Relief Daytime | Haleon US Holdings LLC | 2025-01-01 |
| 00067-0122-01 | 1 KIT in 1 PACKAGE, COMBINATION (0067-0122-01) * 6 PACKET... | Theraflu Severe Cold Relief Combo Pack | Haleon US Holdings LLC | 2024-04-15 |
| 00067-0123-01 | 1 KIT in 1 PACKAGE, COMBINATION (0067-0123-01) * 6 PACKET... | Theraflu Severe Cold Relief Combo Pack | Haleon US Holdings LLC | 2024-06-01 |
| 58933-0552-01 | 5 g in 1 PACKET (58933-552-01) | Vicks DayQuil HOT REMEDY Cold and Flu | Procter & Gamble Manufactura S de RL de CV | 2025-06-11 |
| 58933-0552-08 | 8 PACKET in 1 PACKAGE (58933-552-08) / 5 g in 1 PACKET | Vicks DayQuil HOT REMEDY Cold and Flu | Procter & Gamble Manufactura S de RL de CV | 2025-06-11 |
| 58933-0554-06 | 1 KIT in 1 PACKAGE (58933-554-06) * 5 g in 1 PACKET (58933... | Vicks DayQuil NyQuil HOT REMEDY Cold and Flu | Procter & Gamble Manufactura S de RL de CV | 2025-06-11 |
| 58933-0554-16 | 1 KIT in 1 PACKAGE (58933-554-16) * 5 g in 1 PACKET (58933... | Vicks DayQuil NyQuil HOT REMEDY Cold and Flu | Procter & Gamble Manufactura S de RL de CV | 2025-06-11 |
| 58933-0556-06 | 1 KIT in 1 PACKAGE (58933-556-06) * 1 POWDER, FOR SOLUTION... | Vicks DayQuil NyQuil HOT REMEDY Cold and Flu | Procter & Gamble Manufactura S de RL de CV | 2025-06-11 |
| 58933-0556-16 | 1 KIT in 1 PACKAGE (58933-556-16) * 1 POWDER, FOR SOLUTION... | Vicks DayQuil NyQuil HOT REMEDY Cold and Flu | Procter & Gamble Manufactura S de RL de CV | 2025-06-11 |
| 70264-0047-01 | 25 PACKET in 1 CARTON (70264-047-01) / 1 POWDER, FOR SOLUTI... | Theraflu Severe Cold Relief Daytime | R J General Corporation | 2024-11-12 |
| 79903-0350-12 | 1 KIT in 1 CARTON (79903-350-12) * 6 PACKET in 1 CARTON (7... | WALMART DAYTIME AND NIGHTTIME MS SEVERE RELIEF VALUE PACK | WAL-MART STORES INC | 2026-02-02 |
| 79903-0355-01 | 6 PACKET in 1 CARTON (79903-355-01) / 1 POWDER, FOR SOLUTIO... | Equate Severe Cold and Flu | WALMART INC. | 2026-06-16 |
Observed labelers:
Procter & Gamble Manufactura S de RL de CV (6) ·
Haleon US Holdings LLC (4) ·
R J General Corporation (1) ·
WAL-MART STORES INC (1) ·
WALMART 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.