NDC 54771-2800 - Nolvadent Oral Cleansing

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 54771-2800
Package NDCs from labels: 54771-2800-1, 54771-2800-2
Manufacturer: Zoetis Inc.
Effective date: 2024-02-13
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Nolvadent® Oral Cleansing Solution	Zoetis Inc.	2024-02-13	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
54771-2800-1	Nolvadent Oral Cleansing	118 mL in 1 BOTTLE, PLASTIC	SOLUTION	118		2
54771-2800-2	Nolvadent Oral Cleansing	236 mL in 1 BOTTLE, PLASTIC	SOLUTION	236		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
54771-2800	NOLVADENT ORAL CLEANSING (CHLORHEXIDINE ACETATE) SOLUTION [ZOETIS INC.]	2	2 package rows	20240220_10aa585b-461b-435b-9d08-2771ed779b6c.zip

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 · 3 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Genital Warts Remover Cream	SALICYLIC ACID	Guangxi Keyun E-commerce Co., Ltd.	4c940bec-0a2f-c760-e063-6394a90a30c6	2026-03-09	Warnings	Exact identifier unii: 5908ZUF22Y
iShancare NAIL FUNGUS SERUM	NAIL FUNGUS SERUM	Shenzhen Ishan Technology Co., Ltd	361a61cd-150c-5fcc-e063-6394a90ad553	2026-02-12	Warnings	Exact identifier unii: 5908ZUF22Y
MQUPIN Liquid Fungal Nail Treatment	LIQUID FUNGAL NAIL TREATMENT	Zhengzhou Miaoqi Medical Technology Co., Ltd.	14782f8c-3b29-1d88-e063-6294a90ac3e4	2024-03-25	Warnings	Exact identifier unii: 5908ZUF22Y

Reported adverse events (FAERS/openFDA)#

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