- Active Ingredients
- Purpose
- INDICATIONS & USAGE
- 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 mild to moderate (Stage 2) chronic pain, as indicated by the Homeopathic Pharmacopeia of the United States.
- SPL UNCLASSIFIED SECTION
- Inactive Ingredients:
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
NYLOXIN STAGE 3 PAIN RELIEF
naja naja venom gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47219-253 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (NAJA NAJA VENOM - UNII:ZZ4AG7L7VM) NAJA NAJA VENOM 60 ug in 1 mL Inactive Ingredients Ingredient Name Strength DIPROPYLENE GLYCOL (UNII: E107L85C40) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) 2-(DIETHYLAMINO)ETHANOL (UNII: S6DL4M053U) SODIUM CHLORIDE (UNII: 451W47IQ8X) HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47219-253-20 1 in 1 BOX 1 60 mL in 1 BOTTLE, DISPENSING Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved homeopathic 08/25/2009 Labeler - RECEPTOPHARM INC (145377888) Establishment Name Address ID/FEI Business Operations RECEPTOPHARM INC 145377888 ANALYSIS, MANUFACTURE, API MANUFACTURE Establishment Name Address ID/FEI Business Operations LIQUID PACKAGING RESOURCES 018935165 MANUFACTURE