QUALITY CHOICE

Product NDC: 83324-300
11-digit product format: 833240300
Labeler code: 83324
Product ID: 83324-300_401c4d5c-7ff4-3f9d-e063-6294a90ad71e
Type: HUMAN OTC DRUG
Nonproprietary name: Sodium Citrate dihydrate
Dosage form: TABLET, CHEWABLE
Route: ORAL
Labeler: QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2025-09-15
Substance: TRISODIUM CITRATE DIHYDRATE
Active strength: 230 mg/1
Pharmacologic classes: Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: QUALITY CHOICE
Brand name suffix: Nausea Relief
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
TRISODIUM CITRATE DIHYDRATE	230 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
B22547B95K	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
2002800	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
d89e41c1-399a-4157-8d54-bfefe3b1c1cd	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
83324-300-42	QUALITY CHOICENausea Relief	3 in 1 CARTON	TABLET, CHEWABLE	3		1
83324-300-42	QUALITY CHOICENausea Relief	14 in 1 BLISTER PACK	TABLET, CHEWABLE	14		1

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
QUALITY CHOICE Nausea Relief	SODIUM CITRATE DIHYDRATE	QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)	d89e41c1-399a-4157-8d54-bfefe3b1c1cd	2025-10-01	Warnings	Exact identifier ndc (product): 83324-300

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
B22547B95K	TRISODIUM CITRATE DIHYDRATE	6132-04-3	TRISODIUM CITRATE DIHYDRATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2002800	sodium citrate 230 MG Chewable Tablet	PSN	d89e41c1-399a-4157-8d54-bfefe3b1c1cd	1
2002800	sodium citrate 230 MG Chewable Tablet	SCD	d89e41c1-399a-4157-8d54-bfefe3b1c1cd	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
83324-300-42	83324030042	3 BLISTER PACK in 1 CARTON (83324-300-42) / 14 TABLET, CHEWABLE in 1 BLISTER PACK	3 blister pack	2025-09-15	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Quality Choice Nausea Relief	QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)	2025-10-01	HUMAN OTC DRUG LABEL	1