polyethylene glycol 3350 236000 MG / potassium chloride 2970 MG / sodium bicarbonate 6740 MG / sodium chloride 5860 MG / sodium sulfate 22740 MG Powder for Oral Solution [Gavilyte-G]
RxNorm concept 967012, branded drug (sbd). Prescribable name: Gavilyte-G Powder for Oral Solution.
- RxCUI
- 967012
- Term type
- Branded drug (SBD)
- Status
- Active
curl https://api.healthcare.dev/v1/drugs/rxnorm/967012 \ -H "Authorization: Bearer $HDEV_API_KEY"
Concept
Ingredients and related concepts
Ingredients
- potassium chloride 8591
- sodium chloride 9863
- sodium bicarbonate 36676
- sodium sulfate 36721
- polyethylene glycol 3350 221147
Other names
Gavilyte-G (polyethylene glycol 3350 236 GM / potassium chloride 2.97 GM / sodium bicarbonate 6.74 GM / sodium chloride 5.86 GM / sodium sulfate 22.74 GM) Powder for Oral Solution; POLYETHYLENE GLYCOL 3350 236000 MG / K+ Chloride 2970 MG / NaHCO3 6740 MG / NaCl 5860 MG / sodium sulfate 22740 MG Powder for Oral Solution [Gavilyte-G]; POLYETHYLENE GLYCOL 3350 236000 MG / Pot Chloride 2970 MG / NaHCO3 6740 MG / NaCl 5860 MG / sodium sulfate 22740 MG Powder for Oral Solution [Gavilyte-G]
Related concepts
- polyethylene glycol 3350 236000 MG (SCDC, consists of)
- potassium chloride 2970 MG (SCDC, consists of)
- sodium bicarbonate 6740 MG (SCDC, consists of)
- sodium chloride 5860 MG (SCDC, consists of)
- sodium sulfate 22740 MG (SCDC, consists of)
- polyethylene glycol 3350 236000 MG / potassium chloride 2970 MG / sodium bicarbonate 6740 MG / sodium chloride 5860 MG / sodium sulfate 22740 MG [Gavilyte-G] (SBDC, consists of)
- Powder for Oral Solution (DF, has dose form)
- Gavilyte-G (BN, has ingredient)
- polyethylene glycol 3350 236000 MG / potassium chloride 2970 MG / sodium bicarbonate 6740 MG / sodium chloride 5860 MG / sodium sulfate 22740 MG Powder for Oral Solution (SCD, tradename of)
Linked data
NDCs
NDC-11s RxNorm links to this concept; linked ones open their FDA product.
Use it
Look up 967012 from code or an agent
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Using the healthcare.dev MCP server, look up RxNorm concept 967012. Tell me its name and term type, its ingredients and related concepts, and the NDCs linked to it.
Source: U.S. National Library of Medicine, release 2026-10-05. No license required (Current Prescribable Content). Reference data, not medical advice.