SnoreStop Starter Kit 60

Product NDC: 61152-300
11-digit product format: 611520300
Labeler code: 61152
Product ID: 61152-300_ed769147-dfc1-3ebc-e053-2995a90a9ead
Type: HUMAN OTC DRUG
Nonproprietary name: atropa belladonna,ephedra distachya flowering twig,histamine dihydrochloride,goldenseal,potassium dichromate,strychnos nux-vomica seed,teucrium marum
Dosage form: KIT
Route: NASAL; ORAL
Labeler: Green Pharmaceuticals Inc
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2022-08-01
Marketing end: 0000-00-00
Active strength: 0
NDC exclude flag: No
Listing certified through: 2023-12-31
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 · 4 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	61152-300		I	Inactivated by FDA	2026-10-05
excluded product	product	61152-300		I	Inactivated by FDA	2026-10-05
excluded package	package	61152-300	61152-300-60	I	Inactivated by FDA	2026-10-05
excluded package	package	61152-300	61152-300-77	I	Inactivated by FDA	2026-10-05

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

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
61152-300-60	61152030060	1 KIT in 1 BOX (61152-300-60)	1 kit	2022-08-01	0000-00-00	No	No	Current
61152-300-77	61152030077	1 KIT in 1 BOX (61152-300-77)	1 kit	2022-08-01	0000-00-00	No	No	Current