Emetrol Chewables Mixed Berry

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 Chewables Mixed Berry
Generic name: SODIUM CITRATE DIHYDRATE
Manufacturer: WellSpring Pharmaceutical Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 4965fab0-828d-4f1d-8d43-a636e0a8c1ea
SPL ID: 35e7ffe9-370b-4d46-8019-737ca7238cc6
Version: 2
Effective date: 2023-03-23
Source export date: 2026-10-12
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:26:08

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 Chewables Mixed Berry	openfda.brand_name
generic name		SODIUM CITRATE DIHYDRATE	openfda.generic_name
manufacturer name		WellSpring Pharmaceutical Corporation	openfda.manufacturer_name
ndc	package	65197-420-60	openfda.package_ndc
ndc	product	65197-420	openfda.product_ndc
ndc11	package	65197042060	derived:openfda.package_ndc
rxcui		2596185	openfda.rxcui
rxcui		2002800	openfda.rxcui
spl id		35e7ffe9-370b-4d46-8019-737ca7238cc6	id
spl set id		4965fab0-828d-4f1d-8d43-a636e0a8c1ea	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 Do not use if you have Hereditary Fructose Intolerance (HFI). This product contains fructose. 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 24 tablets 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. In case of overdose, get medical help or contact a Poison Control Center right away. Keep out of reach of children

Reported adverse events (FAERS/openFDA)#

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