FDA.reportPublic FDA data

Nyloxin

Product NDC
47219-300
11-digit product format
472190300
Labeler code
47219
Product ID
47219-300_bbccd2a6-c675-4b2a-a7cf-36fc46580f56
Type
HUMAN OTC DRUG
Nonproprietary name
NAJA NAJA VENOM
Dosage form
GEL
Route
TOPICAL
Labeler
Nutra Pharma Corporation
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2010-08-23
Substance
NAJA NAJA VENOM
Active strength
4 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Nyloxin
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
NAJA NAJA VENOM4 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiZZ4AG7L7VM

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
47219-300-022024-01-30C16284748780-1ba0f9c33-3366-a910-e053-dadaa90a0b85Nyloxin Topical Gel
47219-300-022024-01-30C16284748780-1ba0f9c33-3366-a910-e053-dadaa90a0b85DRUG FACTS
47219-300-082024-01-30C16284748780-1ba0f9c33-1551-a910-e053-dadaa90a0b85DRUG FACTS
47219-300-082024-01-30C16284748780-1ba0f9c33-1551-a910-e053-dadaa90a0b85Nyloxin Topical Gel Professional Size
47219-300-022021-07-14C16284748780-1ba0f9c33-3366-a910-e053-dadaa90a0b85Nyloxin Topical Gel
47219-300-022021-07-14C16284748780-1ba0f9c33-3366-a910-e053-dadaa90a0b85DRUG FACTS
47219-300-082021-07-14C16284748780-1ba0f9c33-1551-a910-e053-dadaa90a0b85DRUG FACTS
47219-300-082021-07-14C16284748780-1ba0f9c33-1551-a910-e053-dadaa90a0b85Nyloxin Topical Gel Professional Size
47219-300-022021-01-29C16284748780-1ba0f9c33-3366-a910-e053-dadaa90a0b85Nyloxin Topical Gel
47219-300-022021-01-29C16284748780-1ba0f9c33-3366-a910-e053-dadaa90a0b85DRUG FACTS
47219-300-082021-01-29C16284748780-1ba0f9c33-1551-a910-e053-dadaa90a0b85DRUG FACTS
47219-300-082021-01-29C16284748780-1ba0f9c33-1551-a910-e053-dadaa90a0b85Nyloxin Topical Gel Professional Size

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47219-300-02Nyloxin60 mL in 1 BOTTLE, DISPENSINGGEL605
47219-300-02Nyloxin1 in 1 BOXGEL15
47219-300-08Nyloxin1 in 1 BOXGEL15
47219-300-08Nyloxin235 mL in 1 BOTTLE, DISPENSINGGEL2355

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
NAJA NAJA VENOMACTIVE INGREDIENTZZ4AG7L7VMNYLOXIN (NAJA NAJA VENOM) GEL [RECEPTOPHARM INC.]1
NAJA NAJA VENOMACTIVE INGREDIENTZZ4AG7L7VMNYLOXIN (NAJA NAJA VENOM) GEL [RECEPTOPHARM INC.]1
NAJA NAJA VENOMACTIVE MOIETYZZ4AG7L7VMNYLOXIN (NAJA NAJA VENOM) GEL [RECEPTOPHARM INC.]1
NAJA NAJA VENOMACTIVE MOIETYZZ4AG7L7VMNYLOXIN (NAJA NAJA VENOM) GEL [RECEPTOPHARM INC.]1
AlcoholINACTIVE INGREDIENT3K9958V90MNYLOXIN (NAJA NAJA VENOM) GEL [RECEPTOPHARM INC.]1
AlcoholINACTIVE INGREDIENT3K9958V90MNYLOXIN (NAJA NAJA VENOM) GEL [RECEPTOPHARM INC.]1
Benzalkonium ChlorideINACTIVE INGREDIENTF5UM2KM3W7NYLOXIN (NAJA NAJA VENOM) GEL [RECEPTOPHARM INC.]1
Benzalkonium ChlorideINACTIVE INGREDIENTF5UM2KM3W7NYLOXIN (NAJA NAJA VENOM) GEL [RECEPTOPHARM INC.]1
Hydroxypropyl CelluloseINACTIVE INGREDIENTRFW2ET671PNYLOXIN (NAJA NAJA VENOM) GEL [RECEPTOPHARM INC.]1
Hydroxypropyl CelluloseINACTIVE INGREDIENTRFW2ET671PNYLOXIN (NAJA NAJA VENOM) GEL [RECEPTOPHARM INC.]1
Propylene GlycolINACTIVE INGREDIENT6DC9Q167V3NYLOXIN (NAJA NAJA VENOM) GEL [RECEPTOPHARM INC.]1
Propylene GlycolINACTIVE INGREDIENT6DC9Q167V3NYLOXIN (NAJA NAJA VENOM) GEL [RECEPTOPHARM INC.]1
Sodium ChlorideINACTIVE INGREDIENT451W47IQ8XNYLOXIN (NAJA NAJA VENOM) GEL [RECEPTOPHARM INC.]1
Sodium ChlorideINACTIVE INGREDIENT451W47IQ8XNYLOXIN (NAJA NAJA VENOM) GEL [RECEPTOPHARM INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47219-300NYLOXIN (NAJA NAJA VENOM) GEL [NUTRA PHARMA CORPORATION]4Current NDC, Legacy NDC, 2 package rows20210715_289ce7d2-9e9e-4792-92b5-de326007da33.zip
47219-300NYLOXIN (NAJA NAJA VENOM) GEL [NUTRA PHARMA CORPORATION]4Current NDC, Legacy NDC, 2 package rows20210715_0ea98615-f6d3-4f74-8faf-c828b7cfc7d3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
47219-300-02472190300021 BOTTLE, DISPENSING in 1 BOX (47219-300-02) / 60 mL in 1 BOTTLE, DISPENSING2010-08-230000-00-00NoNoCurrent
47219-300-08472190300081 BOTTLE, DISPENSING in 1 BOX (47219-300-08) / 235 mL in 1 BOTTLE, DISPENSING2010-08-230000-00-00NoNoCurrent