Severe Anefrin

Product NDC: 0363-2021
11-digit product format: 003632021
Labeler code: 0363
Product ID: 0363-2021_bbb21ead-18db-b1bf-e053-2995a90a1bfc
Type: HUMAN OTC DRUG
Nonproprietary name: OXYMETAZOLINE HYDROCHLORIDE
Dosage form: LIQUID
Route: NASAL
Labeler: WALGREENS
Application: part341
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2021-02-08
Marketing end: 0000-00-00
Substance: OXYMETAZOLINE HYDROCHLORIDE
Active strength: 0 g/15mL
NDC exclude flag: No
Listing certified through: 2022-12-31
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	0363-2021		D	Discontinued by firm		2026-08-11
excluded package	package	0363-2021	0363-2021-15	D	Discontinued by firm		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 · 9 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0363-2021	SEVERE ANEFRIN (OXYMETAZOLINE HYDROCHLORIDE) LIQUID [WALGREENS]	5	Legacy NDC	20241213_b637e03a-dc2b-92a3-e053-2995a90a9a6b.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
K89MJ0S5VY	OXYMETAZOLINE HYDROCHLORIDE	2315-02-8	OXYMETAZOLINE HYDROCHLORIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
0363-2021-15	00363202115	1 BOTTLE, SPRAY in 1 BOTTLE, SPRAY (0363-2021-15) > 15 mL in 1 BOTTLE, SPRAY	2021-02-08	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Severe Anefrin Nasal Spray No Drip MAXIMUM STRENGTH 12 Hour Menthol	WALGREENS	2024-12-11	HUMAN OTC DRUG LABEL	5

Severe Anefrin

NDC auxiliary status#

Observed NDC auxiliary status history#

DailyMed Dashboard NDC Coverage#

Related Records#

Related UNII Ingredients#

Packages#

Related DailyMed Labels#