OHTrust Mouth And Nasal Relief

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	70970-007	70970-007-01	D	Discontinued by firm		2026-10-28

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

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70970-007-01	OHTrust Mouth And Nasal Relief	30 mL in 1 BOTTLE, SPRAY	LIQUID	30		5

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70970-007	OHTRUST MOUTH AND NASAL RELIEF (HYDROXIDE IONS) LIQUID [NANOPLUS LIMITED (CAYMAN) TAIWAN BRANCH]	5	Legacy NDC, 1 package rows	20250212_ddad5680-7310-7c9c-e053-2995a90a5ba3.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
9159UV381P	HYDROXIDE ION	14280-30-9	HYDROXIDE ION

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
70970-007-01	70970000701	30 mL in 1 BOTTLE, SPRAY (70970-007-01)	30 ml	2022-04-28	0000-00-00	No	No	Current