Emetrol Powder Non-Drowsy

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Emetrol Powder Non-Drowsy
Generic name: SODIUM CITRATE DIHYDRATE
Manufacturer: WellSpring Pharmaceutical Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 9d8d2ee7-9db7-4be7-8c73-511eb2e32459
SPL ID: a6121b17-e850-4677-9ad1-ceb36de16336
Version: 3
Effective date: 2025-01-08
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:53:53

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Emetrol Powder Non-Drowsy	openfda.brand_name
generic name		SODIUM CITRATE DIHYDRATE	openfda.generic_name
manufacturer name		WellSpring Pharmaceutical Corporation	openfda.manufacturer_name
ndc	package	65197-203-09	openfda.package_ndc
ndc	product	65197-203	openfda.product_ndc
ndc11	package	65197020309	derived:openfda.package_ndc
rxcui		2671579	openfda.rxcui
rxcui		2671573	openfda.rxcui
spl id		a6121b17-e850-4677-9ad1-ceb36de16336	id
spl set id		9d8d2ee7-9db7-4be7-8c73-511eb2e32459	set_id
unii		B22547B95K	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Ask a doctor before use if you have diabetes because this product contains sugar are on a sodium-restricted diet Ask a doctor or pharmacist before use if you are taking any other medications. This product may interact with certain prescription drugs. When using this product, do not take more than 4 packets in a 24-hour period. Stop use and ask a doctor if nausea lasts more than two weeks or recurs frequently. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children In case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.