Ammonia Inhalants

Product NDC: 0273-0104
11-digit product format: 002730104
Labeler code: 0273
Product ID: 0273-0104_f1621e06-f87b-2afa-e053-2a95a90a90e4
Type: HUMAN OTC DRUG
Nonproprietary name: Ammonia Inhalants
Dosage form: INHALANT
Route: RESPIRATORY (INHALATION)
Labeler: YOUNG DENTAL MANUFACTURING CO 1, LLC
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2018-01-09
Marketing end: 0000-00-00
Substance: AMMONIA
Active strength: 0 g/.3mL
NDC exclude flag: No
Listing certified through: 2024-12-31
Current FDA listing: Historical FDA.report record

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	0273-0104		I	Inactivated by FDA		2026-08-11
excluded package	package	0273-0104	0273-0104-10	I	Inactivated by FDA		2026-08-11

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 18 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	0273-0104-10	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	0273-0104-10	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	0273-0104-10	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	0273-0104-10	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	0273-0104-10	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	0273-0104-10	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	0273-0104-10	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	0273-0104-10	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	0273-0104-10	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0273-0104-10	2025-01-30	C162847	48780-1	2cef2736-89ba-d83d-e063-dadaa90ab31f	AMMONIA INHALER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0273-0104-10	Ammonia Inhalants	0.3 mL in 1 AMPULE	INHALANT	0.3		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0273-0104	AMMONIA INHALANTS INHALANT [YOUNG DENTAL MANUFACTURING CO 1, LLC]	5	Legacy NDC, 1 package rows	20230105_5d83b8c0-914c-4ad4-a1c6-45215bfacbd8.zip

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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1299889	ammonia 15 % Nasal Inhalant	PSN	5d83b8c0-914c-4ad4-a1c6-45215bfacbd8	5
1299889	ammonia 150 MG/ML Nasal Inhalant	SCD	5d83b8c0-914c-4ad4-a1c6-45215bfacbd8	5
1299889	ammonia 0.045 GM per 0.3 ML Nasal Inhalant	SY	5d83b8c0-914c-4ad4-a1c6-45215bfacbd8	5
1299889	ammonia 0.3 ML Nasal Inhalant	SY	5d83b8c0-914c-4ad4-a1c6-45215bfacbd8	5
1299889	ammonia 15 % Nasal Inhalant	SY	5d83b8c0-914c-4ad4-a1c6-45215bfacbd8	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
0273-0104-10	00273010410	.3 mL in 1 AMPULE (0273-0104-10)	2018-01-10	0000-00-00	No	No	Current