NYLOXIN

Product NDC
47219-203
11-digit product format
472190203
Labeler code
47219
Product ID
47219-203_4817aae0-ddc5-11de-a5b9-0002a5d5c51b
Type
HUMAN OTC DRUG
Nonproprietary name
NAJA NAJA VENOM
Dosage form
SPRAY, METERED
Route
ORAL
Labeler
RECEPTOPHARM INC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-08-25
Marketing end
0000-00-00
Substance
NAJA NAJA VENOM
Active strength
0 mg/mL
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
47219-203-102019-10-21C16284748780-1956f9ecf-d4df-621f-e053-dbdaa90a74adDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47219-203-10NYLOXINStage 2 Pain Relief15 mL in 1 BOTTLE, SPRAYSPRAY, METERED151
47219-203-10NYLOXINStage 2 Pain Relief1 in 1 BOXSPRAY, METERED11

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47219-203NYLOXIN STAGE 2 PAIN RELIEF (NAJA NAJA VENOM) SPRAY, METERED [RECEPTOPHARM INC]1Legacy NDC, 2 package rows20110113_9ad47340-ddbf-11de-a1c2-0002a5d5c51b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
47219-203-104721902031015 mL in 1 BOTTLE, SPRAY15 mlHistorical