Palinoia Ammonia Inhalant

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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	87176-002		D	Discontinued by firm		2026-08-11
excluded package	package	87176-002	87176-002-02	D	Discontinued by firm		2026-08-11

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
87176-002-01	Palinoia Ammonia Inhalant	40 g in 1 BOTTLE	INHALANT	40		3
87176-002-02	Palinoia Ammonia Inhalant	1 in 1 BOX	INHALANT	1		3

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5138Q19F1X	AMMONIA	7664-41-7	AMMONIA

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1299889	ammonia 15 % Nasal Inhalant	PSN	42699816-1ae2-cfea-e063-6394a90aec1f	3
1299889	ammonia 150 MG/ML Nasal Inhalant	SCD	42699816-1ae2-cfea-e063-6394a90aec1f	3
1299889	ammonia 0.045 GM per 0.3 ML Nasal Inhalant	SY	42699816-1ae2-cfea-e063-6394a90aec1f	3
1299889	ammonia 0.3 ML Nasal Inhalant	SY	42699816-1ae2-cfea-e063-6394a90aec1f	3
1299889	ammonia 15 % Nasal Inhalant	SY	42699816-1ae2-cfea-e063-6394a90aec1f	3

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
87176-002-01	87176000201	40 g in 1 BOTTLE	40 g				Historical
87176-002-02	87176000202	1 BOTTLE in 1 BOX (87176-002-02) / 40 g in 1 BOTTLE (87176-002-01)	1 bottle	2025-11-01	No	No	Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
COTTON - Centeroblivion LLC \| Guangzhou Ludingji Biotechnology Co.,Ltd.	Centeroblivion LLC \| Guangzhou Ludingji Biotechnology Co.,Ltd.	2026-05-03	HUMAN OTC DRUG LABEL	3