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NDC 47219-0311-02 Nyloxin 4 [hp_X]/mL Details
Nyloxin 4 [hp_X]/mL
Nyloxin is a TOPICAL GEL in the HUMAN OTC DRUG category. It is labeled and distributed by Nutra Pharma Corporation. The primary component is NAJA NAJA VENOM.
Product Information
NDC | 47219-0311 |
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Product ID | 47219-311_c71b3c68-d5d0-6e4f-e053-2a95a90ab98f |
Associated GPIs | |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | Nyloxin |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | NAJA NAJA VENOM |
Product Type | HUMAN OTC DRUG |
Dosage Form | GEL |
Route | TOPICAL |
Active Ingredient Strength | 4 |
Active Ingredient Units | [hp_X]/mL |
Substance Name | NAJA NAJA VENOM |
Labeler Name | Nutra Pharma Corporation |
Pharmaceutical Class | n/a |
DEA Schedule | n/a |
Marketing Category | UNAPPROVED HOMEOPATHIC |
Application Number | n/a |
Listing Certified Through | 2022-12-31 |
Package
Package Images


NDC 47219-0311-02 (47219031102)
NDC Package Code | 47219-311-02 |
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Billing NDC | 47219031102 |
Package | 1 BOTTLE, WITH APPLICATOR in 1 BOX (47219-311-02) / 60 mL in 1 BOTTLE, WITH APPLICATOR |
Marketing Start Date | 2010-08-23 |
NDC Exclude Flag | N |
Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL c28c50db-4b6b-4307-8fcb-9020d6ae9cd3 Details
Purpose
Warnings:
Directions for Use:
Other Information:
- Do not use if container seal is broken prior to opening.
- This product is intended for use in cases of recurring joint pain.
- This product is NOT intended to treat disease, it provides a temporary level of comfort, relief and a feeling of wellness.
- This product has been determined to be safe and effective for moderate to severe (Stage 2) chronic pain, as indicated by the Homeopathic Pharmacopeia of the United States.
SPL UNCLASSIFIED SECTION
SPL UNCLASSIFIED SECTION
INGREDIENTS AND APPEARANCE
NYLOXIN
naja naja venom gel |
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Labeler - Nutra Pharma Corporation (141236286) |
Revised: 7/2021
Document Id: c71b3c68-d5d0-6e4f-e053-2a95a90ab98f
Set id: c28c50db-4b6b-4307-8fcb-9020d6ae9cd3
Version: 4
Effective Time: 20210714