Home NDC 47219-301-02 Nyloxin
Product NDC 47219-301
Requested package NDC 47219-301-02
11-digit product format 472190301
Labeler code 47219
Product ID 47219-301_45ca5222-6d69-4184-90b6-e1dcf4bf2ce2
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 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 · 14 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 2025-08-27 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…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Additional Listing Data#
Finished product Yes
Brand name base Nyloxin
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength NAJA NAJA VENOM 4 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination ZZ4AG7L7VM Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 47219-301-02 Nyloxin 60 mL in 1 BOTTLE, WITH APPLICATOR GEL 60 5 47219-301-02 Nyloxin 1 in 1 BOX GEL 1 5
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 47219-301 NYLOXIN (NAJA NAJA VENOM) GEL [NUTRA PHARMA CORPORATION] 4 Current NDC, Legacy NDC, 2 package rows 20210715_452ca1bf-6c32-45b5-9574-3da8bb71757d.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 47219-301-02 47219030102 1 BOTTLE, WITH APPLICATOR in 1 BOX (47219-301-02) / 60 mL in 1 BOTTLE, WITH APPLICATOR 2010-08-23 0000-00-00 No No Current