NDC 46066-200 - BLOAT TREATMENT

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: 46066-200
Package NDCs from labels: 46066-200-04
Manufacturer: Aspen Veterinary Resources, Ltd
Effective date: 2022-01-03
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
BLOAT TREATMENT - Aspen Veterinary Resources, Ltd	Aspen Veterinary Resources, Ltd	2022-01-03	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
46066-200-04	BLOAT TREATMENT	354.9 mL in 1 BOTTLE	EMULSION	354.9		7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
46066-200	BLOAT TREATMENT (DOCUSATE SODIUM) EMULSION [ASPEN VETERINARY RESOURCES, LTD]	7	1 package rows	20220104_1b866156-706b-41ba-b5f6-0fc1ed2ff5f8.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 17 of 17 · 323 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Stool Softener	DOCUSATE SODIUM	Allegiant Health	30c9ff75-cee4-4632-86fd-acfdf5ee85af	2020-10-27	Warnings	Exact identifier unii: F05Q2T2JA0
Stool Softener	MARC GLASSMAN	Marc Glassman, Inc.	909cd222-d836-416f-aa7d-deb4a0c5a560	2020-09-08	Warnings	Exact identifier unii: F05Q2T2JA0
STOOL SOFTENING SENNA LAXATIVE	SENNOSIDES 8.6 MG - DOCUSATE SODIUM 50 MG	TARGET CORPORATION	7c74bd91-6687-2b89-e053-2a91aa0ad6b8	2019-02-28	Warnings	Exact identifier unii: F05Q2T2JA0

Reported adverse events (FAERS/openFDA)#

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